UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549



FORM 10-Q



(Mark One)

QUARTERLY REPORT PURSUANT TO SECTION13 OR 15(d)OF THE SECURITIES EXCHANGE ACT OF 1934

For the quarterly period ended SeptemberJune 30, 20172022

TRANSITION REPORT UNDER SECTION13 OR 15(d)OF THE SECURITIES EXCHANGE ACT OF 1934


For the transition period fromto


Commission file number: 000-55473001-38659


BIOSIG TECHNOLOGIES, INC.

(Exact name of registrant as specified in its charter)


Delaware

26-4333375

Delaware

26-4333375

(State or other jurisdiction of incorporation

or organization)

(I.R.S.IRS Employer Identification No.)

55 Greens Farms Road, 1st Floor

Westport, CT

06880

(Address of principal executive office)

(Zip Code)

(203) 409-5444

(Registrant’s telephone number, including area code)


8441 Wayzata Blvd, Suite 240
Minneapolis, MN 55426
(Address

Securities registered pursuant to Section 12(b) of principal executive offices) (zip code)the Act:

Title of each class

Trading Symbol(s)

Name of each exchange on which registered

Common Stock, par value $0.001 per share

BSGM

The NASDAQ Capital Market


(763) 999-7331
(Registrant’s telephone number, including area code)

Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days. Yes No


Indicate by check mark whether the registrant has submitted electronically and posted on its corporate Web site, if any, every Interactive Data File required to be submitted and posted pursuant to Rule 405 of Regulation S-T (§ 232.405229.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit and post such files). Yes No


Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, a smaller reporting company, or an emerging growth company. See definitions of “large accelerated filer,” “accelerated filer,” “smaller reporting company,” and “emerging growth company” in Rule 12b-2 of the Exchange Act.

Large accelerated filer

Accelerated filer

Non-accelerated filer

Smaller reporting company

Emerging growth company

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.


Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act). Yes No



PART 1 I FINANCIAL INFORMATION


ITEM 1. FINANCIAL STATEMENTS


BIOSIG TECHNOLOGIES, INC. 
CONDENSED BALANCE SHEETS
 
  
  September 30,  December 31, 
  2017  2016 
  (unaudited)    
ASSETS      
Current assets:      
Cash $234,285  $1,055,895 
Prepaid expenses  150,482   134,263 
  Total current assets  384,767   1,190,158 
         
Property and equipment, net  18,866   24,188 
         
Other assets:        
Deposits  19,473   27,612 
         
  Total assets $423,106  $1,241,958 
         
LIABILITIES AND STOCKHOLDERS' DEFICIT        
Current liabilities:        
Accounts payable and accrued expenses, including $17,888 and $15,755 to related parties as of September 30, 2017 and December 31, 2016, respectively $1,301,603  $373,103 
Dividends payable  396,939   359,891 
Warrant liability  2,240,510   1,937,234 
Derivative liability  285,032   288,934 
  Total current  liabilities  4,224,084   2,959,162 
         
Series C Preferred Stock, 985 and 1,070 shares issued and outstanding; liquidation preference of $985,000 and $1,070,000 as of September 30, 2017 and December 31, 2016, respectively  985,000   1,070,000 
         
Stockholders' deficit        
Preferred stock, $0.001 par value, authorized 1,000,000 shares, designated 200 shares of Series A, 600 shares of Series B and 4,200 shares of Series C Preferred Stock        
Common stock, $0.001 par value, authorized 200,000,000 shares, 26,413,745 and 22,588,184 issued and outstanding as of September 30, 2017 and December 31, 2016, respectively  26,414   22,588 
Additional paid in capital  46,888,447   41,019,251 
Common stock subscription  279,940   - 
Accumulated deficit  (51,980,779)  (43,829,043)
  Total stockholders' deficit  (4,785,978)  (2,787,204)
         
Total liabilities and stockholders' deficit $423,106  $1,241,958 

BIOSIG TECHNOLOGIES, INC.

CONDENSED CONSOLIDATED BALANCE SHEETS

(In Thousands, Except Par Value and Share Amounts)

  

June 30,

  

December 31,

 
  

2022

  

2021

 
  

(unaudited)

     

ASSETS

        

Current assets:

        

Cash

 $5,077  $11,659 

Inventory

  2,026   1,881 

Prepaid expenses and vendor deposits

  633   354 

Total current assets

  7,736   13,894 
         

Property and equipment, net

  596   652 
         

Right-to-use assets, net

  898   604 
         

Other assets:

        

Patents, net

  317   326 

Trademarks

  1   1 

Deposits

  42   42 
         

Total assets

 $9,590  $15,519 
         

LIABILITIES AND EQUITY

        

Current liabilities:

        

Accounts payable and accrued expenses, including $104 and $86 to related parties as of June 30, 2022 and December 31, 2021, respectively

 $1,451  $2,179 

Deferred revenue, short term

  21   32 

Dividends payable

  86   82 

Lease liability, short term

  341   283 

Total current liabilities

  1,899   2,576 
         

Deferred revenue, long term

  -   5 

Lease liability, long term

  609   373 

Total long-term liabilities

  609   378 
         

Total liabilities

  2,508   2,954 
         

Commitments and contingencies (Note 10)

        
         

Series C 9% Convertible Preferred Stock, $0.001 par value, $1,000 stated value, authorized 4,200 shares, 105 shares issued and outstanding: liquidation preference of $105 as of June 30, 2022 and December 31, 2021

  105   105 
         

Equity:

        

Preferred stock, $0.001 par value, authorized 1,000,000 shares, designated 200 shares of Series A, 600 shares of Series B, 4,200 shares of Series C, 1,400 shares of Series D, 1,000 shares of Series E, 200,000 shares of Series F Preferred Stock, none issued

  -   - 

Common stock, $0.001 par value, authorized 200,000,000 shares, 44,811,880 and 35,567,180 issued and outstanding as of June 30, 2022 and December 31, 2021, respectively

  45   36 

Additional paid in capital

  209,456   201,127 

Accumulated deficit

  (202,644)  (188,922)

Total stockholders' equity attributable to BioSig Technologies, Inc.

  6,857   12,241 

Non-controlling interest

  120   219 

Total equity

  6,977   12,460 
         

Total liabilities and equity

 $9,590  $15,519 

See the accompanying notes to the unaudited condensed consolidated financial statements


BIOSIG TECHNOLOGIES, INC. 
CONDENSED STATEMENTS OF OPERATIONS
 
(unaudited) 
             
  Three months ended September 30,  Nine months ended September 30, 
  2017  2016  2017  2016 
Operating expenses:            
Research and development $1,124,506  $560,514  $3,802,149  $2,139,671 
General and administrative  786,948   991,852   4,020,625   7,257,852 
Depreciation  2,834   2,570   8,900   7,811 
  Total operating expenses  1,914,288   1,554,936   7,831,674   9,405,334 
                 
Loss from operations  (1,914,288)  (1,554,936)  (7,831,674)  (9,405,334)
                 
Other income (expense):                
Gain (loss) on change in fair value of derivatives  113,724   17,771   (320,131)  (807,087)
Interest income  15   -   69   1 
                 
Loss before income taxes  (1,800,549)  (1,537,165)  (8,151,736)  (10,212,420)
                 
Income taxes (benefit)  -   -   -   - 
                 
Net loss  (1,800,549)  (1,537,165)  (8,151,736)  (10,212,420)
                 
Preferred stock dividend  (22,307)  (24,726)  (68,915)  (85,467)
                 
NET LOSS AVAILABLE TO COMMON STOCKHOLDERS $(1,822,856) $(1,561,891) $(8,220,651) $(10,297,887)
                 
Net loss per common share, basic and diluted $(0.07) $(0.08) $(0.33) $(0.55)
                 
Weighted average number of common shares outstanding, basic and diluted  26,071,408   20,581,041   24,762,649   18,847,515 

BIOSIG TECHNOLOGIES, INC.

CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS

(In Thousands, Except Par Value and Share Amounts)

(unaudited)

  

Three months ended June 30,

  

Six months ended June 30,

 
  

2022

  

2021

  

2022

  

2021

 

Revenue:

                

Product sales

 $-  $199  $-  $314 

Service

  8   8   16   11 

Total revenue

  8   207   16   325 
                 

Cost of goods sold

  -   62   -   161 
                 

Gross profit

  8   145   16   164 
                 

Operating expenses:

                

Research and development

  1,351   1,667   2,968   2,933 

General and administrative

  4,302   6,480   10,703   13,751 

Depreciation and amortization

  71   49   126   91 

Total operating expenses

  5,724   8,196   13,797   16,775 
                 

Loss from operations

  (5,716)  (8,051)  (13,781)  (16,611)
                 

Other income (expense):

                

Interest income, net

  -   -   -   1 
                 

Loss before income taxes

  (5,716)  (8,051)  (13,781)  (16,610)
                 

Income taxes (benefit)

  -   -   -   - 
                 

Net loss

  (5,716)  (8,051)  (13,781)  (16,610)
                 

Non-controlling interest

  (43)  350   59   590 
                 

Net loss attributable to BioSig Technologies, Inc.

  (5,759)  (7,701)  (13,722)  (16,020)
                 

Preferred stock dividend

  (3)  (3)  (5)  (5)

Preferred stock deemed dividend

  (108)  -   (108)  - 
                 

NET LOSS ATTRIBUTABLE TO COMMON SHAREHOLDERS

 $(5,870) $(7,704) $(13,835) $(16,025)
                 

Net loss per common share, basic and diluted

 $(0.15) $(0.24) $(0.36) $(0.50)
                 

Weighted average number of common shares outstanding, basic and diluted

  39,823,034   32,169,191   37,920,734   31,878,283 

See the accompanying notes to the unaudited condensed consolidated financial statements



BIOSIG TECHNOLOGIES, INC. 
CONDENSED STATEMENT OF STOCKHOLDERS' DEFICIT
 
NINE MONTHS ENDED SEPTEMBER 30, 2017 
                   
        Additional          
  Common stock  Paid in  Common stock  Accumulated    
  Shares  Amount  Capital  Subscription  Deficit  Total 
Balance, December 31, 2016  22,588,184  $22,588  $41,019,251  $-  $(43,829,043) $(2,787,204)
Sale of common stock  2,870,865   2,871   4,118,033   -   -   4,120,904 
Common stock issued for services  625,000   625   894,124   -   -   894,749 
Common stock issued upon conversion of Series C Preferred Stock at $1.50 per share  56,669   57   84,943   -   -   85,000 
Common stock issued settlement of Series C Preferred Stock accrued dividends at $1.37 per share  24,021   24   31,844   -   -   31,868 
Common stock received and canceled in connection with short term swing profit reimbursement  (10,744)  (11)  11   -   -   - 
Common stock subscription received  -   -   -   279,940   -   279,940 
Reclassify fair value of derivative liability to equity upon conversion of Series C Preferred Stock to common shares  -   -   20,757   -   -   20,757 
Fair value of warrant issued to acquire research and development  -   -   543,927   -   -   543,927 
Stock based compensation  259,750   260   244,472   -   -   244,732 
Preferred stock dividend  -   -   (68,915)  -   -   (68,915)
Net loss  -   -   -   -   (8,151,736)  (8,151,736)
  Balance, September 30, 2017 (unaudited)  26,413,745  $26,414  $46,888,447  $279,940  $(51,980,779) $(4,785,978)

BIOSIG TECHNOLOGIES, INC.

CONDENSED CONSOLIDATED STATEMENT OF CHANGES IN EQUITY

THREE AND SIX MONTHS ENDED JUNE 30, 2022

(In Thousands, Except Par Value and Share Amounts)

  

Common stock

  

Additional

Paid in

  

Accumulated

  

Non-controlling

     
  

Shares

  

Amount

  

Capital

  

Deficit

  

Interest

  

Total

 

Balance, December 31, 2021

  35,567,180  $36  $201,127  $(188,922) $219  $12,460 

Common stock issued for services

  1,312,500   1   1,600   -   -   1,601 

Change in fair value of modified options

  -   -   15   -   -   15 

Sale of common stock and warrants, net transactional costs of $3

  2,613,130   2   3,000   -   -   3,002 

Stock based compensation

  66,249   *   500   -   (101)  399 

Preferred stock dividend

  -   -   (2)  -   -   (2)

Net loss

  -   -   -   (7,963)  (102)  (8,065)

Balance, March 31, 2022 (unaudited)

  39,559,059   39   206,240   (196,885)  16   9,410 

Common stock issued for services

  567,500   1   482   -   -   483 

Sale of common stock under At-the-market offering, net of transaction expenses of $46

  322,404   *   302   -   -   302 

Sale of common stock, net transactional costs of $438

  4,341,667   5   2,813   -   -   2,818 

Issuance of subsidiary stock in settlement of debt to parent

  -   -   (292)      292   - 

Stock based compensation

  21,250   *   (86)  -   (231)  (317)

Accretion of deemed preferred stock dividend

  -   -   108   -   -   108 

Deemed preferred stock dividend

  -   -   (108)  -   -   (108)

Preferred stock dividend

  -   -   (3)  -   -   (3)

Net loss

  -   -   -   (5,759)  43   (5,716)

Balance, June 30, 2022 (unaudited)

  44,811,880  $45  $209,456  $(202,644) $120  $6,977 

See the accompanying notes to the unaudited condensed consolidated financial statements



BIOSIG TECHNOLOGIES, INC. 
CONDENSED STATEMENTS OF CASH FLOWS
 
(unaudited) 
       
  Nine months ended September 30, 
  2017  2016 
CASH FLOWS FROM OPERATING ACTIVITIES:      
Net loss $(8,151,736) $(10,212,420)
Adjustments to reconcile net loss to cash used in operating activities:        
Depreciation  8,900   7,811 
Equipment distribution as officer compensation  3,210   - 
Change in derivative liabilities  320,131   807,087 
Equity based compensation  1,139,481   5,453,240 
Fair value of issued warrant to acquire research and development  543,927   - 
Changes in operating assets and liabilities:        
Prepaid expenses  (16,219)  (103,222)
Security deposit  8,139   - 
Accounts payable  930,110   202,534 
Deferred rent payable  (1,609)  417 
  Net cash used in operating activities  (5,215,666)  (3,844,553)
         
CASH FLOWS FROM INVESTING ACTIVITIES:        
Purchase of property and equipment  (6,788)  (12,095)
  Net cash used in investing activity  (6,788)  (12,095)
         
CASH FLOWS FROM FINANCING ACTIVITIES:        
Proceeds from sale of common stock  4,120,904   3,053,868 
Proceeds from common stock subscription  279,940   - 
  Net cash provided by financing activities  4,400,844   3,053,868 
         
Net decrease in cash and cash equivalents  (821,610)  (802,780)
         
Cash and cash equivalents, beginning of the period  1,055,895   953,234 
Cash and cash equivalents, end of the period $234,285  $150,454 
         
Supplemental disclosures of cash flow information:        
Cash paid during the period for interest $-  $- 
Cash paid during the period for income taxes $-  $- 
         
Non cash investing and financing activities:        
Common stock issued upon conversion of Series C Preferred Stock and accrued dividends $116,868  $465,355 
Reclassify fair value of derivative liability to equity $20,757  $97,897 

BIOSIG TECHNOLOGIES, INC.

CONDENSED CONSOLIDATED STATEMENT OF CHANGES IN EQUITY

THREE AND SIX MONTHS ENDED JUNE 30, 2021

(In Thousands, Except Par Value and Share Amounts)

  

Common stock

  

Additional

Paid in

  

Accumulated

  

Non-controlling

     
  

Shares

  

Amount

  

Capital

  

Deficit

  

Interest

  

Total

 

Balance, December 31, 2020

  30,764,792  $31  $181,344  $(157,005) $802  $25,172 

Common stock issued for services

  406,692   *   1,777   -   -   1,777 

Common stock issued upon exercise of options at $2.96 per share

  9,375   *   28   -   -   28 

Sale of common stock under At-the-market offering, net of transaction expenses of $40

  251,720   *   1,300   -   -   1,300 

Stock based compensation

  682,202   1   721   -   20   742 

Preferred stock dividend

  -   -   (2)  -   -   (2)

Net loss

  -   -   -   (8,319)  (240)  (8,559)

Balance, March 31, 2021 (unaudited)

  32,114,781   32   185,168   (165,324)  582   20,458 

Common stock issued for services

  36,948   *   140   -   -   140 

Change in fair value of modified options

  -   -   313   -   8   321 

Stock based compensation

  53,750   *   1,518   -   134   1,652 

Preferred stock dividend

  -   -   (3)  -   -   (3)

Net loss

  -   -   -   (7,701)  (350)  (8,051)

Balance, June 30, 2021 (unaudited)

  32,205,479  $32  $187,136  $(173,025) $374  $14,517 

See the accompanying notes to the unaudited condensed consolidated financial statements



BIOSIG TECHNOLOGIES, INC.

CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS

(In Thousands, Except Par Value and Share Amounts)

(unaudited)

  

Six months ended June 30,

 
  

2022

  

2021

 

CASH FLOWS FROM OPERATING ACTIVITIES:

        

Net loss

 $(13,781) $(16,610)

Adjustments to reconcile net loss to cash used in operating activities:

        

Depreciation and amortization

  126   91 

Non-cash lease expense

  166   230 

Equity based compensation

  2,166   4,311 

Change in fair value of modified options

  15   321 

Changes in operating assets and liabilities:

        

Accounts receivable

  -   (199)

Inventory

  (145)  37 

Prepaid expenses and other

  (277)  (209)

Deferred revenue

  (16)  53 

Accounts payable and accrued expenses

  (731)  (1,693)

Operating lease liabilities

  (167)  (242)

Net cash used in operating activities

  (12,644)  (13,910)
         

CASH FLOWS FROM INVESTING ACTIVITIES:

        

Purchase of property and equipment

  (60)  (182)

Net cash used in investing activity

  (60)  (182)
         

CASH FLOWS FROM FINANCING ACTIVITIES:

        

Proceeds from sale of common stock, net of issuance costs

  5,820   - 

Proceeds from sale of common stock under a At-the-market offering, net of issuance costs

  302   1,300 

Proceeds from exercise of options

  -   28 

Net cash provided by financing activities

  6,122   1,328 
         

Net decrease in cash and cash equivalents

  (6,582)  (12,764)
         

Cash, beginning of the period

  11,659   28,268 

Cash, end of the period

 $5,077  $15,504 
         

Supplemental disclosures of cash flow information:

        

Cash paid during the period for interest

 $-  $- 

Cash paid during the period for income taxes

 $-  $- 
         

Noncash investing and financing activities:

        

Dividend payable on preferred stock charged to additional paid in capital

 $5  $5 

Series C convertible preferred stock deemed dividend

 $108  $- 

Record right-to-use assets and related lease liability

 $502  $218 

See the accompanying notes to the unaudited condensed consolidated financial statements

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

SEPTEMBER

JUNE 30, 20172022

(unaudited)

(unaudited)


NOTE 1 NATURE OF OPERATIONS AND BASIS OF PRESENTATION


Business and organization

BioSig Technologies, Inc. (the “Company”) was initially incorporated on February 24, 2009 under the laws of the State of Nevada and subsequently re-incorporated in the state of Delaware in 2011. The Company is principally devoted to improving the qualitystandard care in electrophysiology with our PURE EP System’s enhanced signal acquisition, digital signal processing, and analysis during ablation of cardiac recordings obtained during EP studies and catheter ablation procedures.arrhythmias. The Company has not generated anyminimal revenue to date and consequently its operations are subject to all risks inherent in business enterprises in early commercialization stage.

On November 7, 2018, the establishmentCompany formed a subsidiary under the laws of the State of Delaware originally under the name of NeuroClear Technologies, Inc. which was renamed to ViralClear Pharmaceuticals, Inc. (“ViralClear”) in March 2020. The subsidiary was established to pursue additional applications of the PURE EP™ signal processing technology outside of cardiac electrophysiology, and subsequently in 2020, was repurposed to develop merimepodib, a new business enterprise.broad-spectrum anti-viral agent that showed potential for the treatment of COVID-19. Since late 2020, ViralClear has been realigned with its original objective of pursuing additional applications of the PURE EP™ signal processing technology outside of cardiac electrophysiology.

As of June 30, 2022, the Company had a majority interest in ViralClear of 69.08%.

On July 2, 2020, the Company formed an additional subsidiary, NeuroClear Technologies, Inc., a Delaware corporation.

The unaudited condensed interimconsolidated financial statements include the accounts of BioSig Technologies, Inc., its wholly owned subsidiary, NeuroClear Technologies, Inc. and its majority owned subsidiary, ViralClear Pharmaceuticals, Inc. as the “Company” or “BioSig”.

The unaudited condensed consolidated financial statements of the Company have been prepared in accordance with accounting principles generally accepted in the United States (“GAAP”) for interim financial information and the instructions to Form 10-Q and Rule 8-03 of Regulation S-X. Accordingly, they do not include all of the information and footnotes required by GAAP for complete financial statements. In the opinion of management, all adjustments (consisting of normal recurring accruals) considered necessary for a fair presentation have been included.

The condensed consolidated balance sheet as of December 31, 20162021 has been derived from audited financial statements.

Operating results for the three and ninesix months ended SeptemberJune 30, 20172022 are not necessarily indicative of results that may be expected for the year ending December 31, 2017.2022. These unaudited condensed consolidated financial statements should be read in conjunction with the audited financial statements for the year ended December 31, 20162021 filed with the Company’s Form 10-K with the Securities and Exchange Commission on March 31, 2022.

COVID-19

On March 11, 2020, the World Health Organization declared a pandemic related to the rapidly spreading coronavirus (COVID-19) outbreak, which has led to a global health emergency. The full public-health impact of the ongoing pandemic is currently indeterminable and rapidly evolving, and the related health crisis has adversely affected and may continue to adversely affect the global economy, resulting in delays to our commercialization objectives of the PURE EP Systems into 2022.

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2017.2022

(unaudited)


NOTE 2 GOING CONCERN AND MANAGEMENT’SMANAGEMENTS LIQUIDITY PLANS


As of SeptemberJune 30, 2017,2022, the Company had cash of $234,285$5.1 million and working capital deficit (current liabilities in excess of current assets) of $3,839,317 principally due to$5.8 million. During the inclusion of non-cash derivative and warrant liabilities recorded in current liabilities. In addition, the Company raised approximately $4,401,000 in ninesix months ended SeptemberJune 30, 2017 through the sale of common stock and warrants and approximately $2,850,000 subsequent to September 30, 2017 (See Note 12). As of September 30, 2017, excluding the derivative and warrant liabilities, the Company’s working capital deficit would have been $1,313,775. During the nine months ended September 30, 2017,2022, the Company used net cash in operating activities of $5,215,666.$12.6 million. These conditions raise substantial doubt about the Company’s ability to continue as a going concern. Management believes that the Company has sufficient funds to meet its research and development and other funding requirements for at least the next 4 months.


The Company’s primary source of operating funds since inception has been cash proceeds from private placementssale of common and preferred stock. The Company has experienced net losses and negative cash flows from operations since inception and expects these conditions to continue for the foreseeable future.

The Company’s plans include the continued commercialization of the PURE EP System and other applications of our core technology and raising capital through the sale of additional equity securities, debt or capital inflows from strategic partnerships. The Company’s strategic shift from a focus on technology development to commercialization will allow the Company to significantly reduce operating expenses.

The Company has stockholders’ deficiencies at September 30, 2017 and requireswill require additional financing to fund future operations. Further, although the Company does not have anybegan commercial products available for sale andoperations; there is no assurance that if approval of their products is received that the Company will be able to generate sufficient cash flow to fund operations. In addition, there can be no assurance that the Company’s continuing research and development will be successfully completed or that any productadditional products will be approved or commercially viable.


Accordingly, the accompanying unaudited condensed consolidated financial statements have been prepared in conformity with U.S. GAAP, which contemplates continuation of the Company as a going concern and the realization of assets and satisfaction of liabilities in the normal course of business. The carrying amounts of assets and liabilities presented in the unaudited condensed consolidated financial statements do not necessarily purport to represent realizable or settlement values. The unaudited condensed consolidated financial statements do not include any adjustment that might result from the outcome of this uncertainty.


BIOSIG TECHNOLOGIES, INC.
NOTES TO THE CONDENSED FINANCIAL STATEMENTS
SEPTEMBER 30, 2017
(unaudited)

NOTE 3 –SUMMARY SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES


Use of estimatesEstimates


The preparation of these unaudited condensed consolidated financial statements in conformity with GAAP requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities, disclosure of contingent assets and liabilities at the date of the consolidated financial statements and the reported amounts of revenues and expenses during the reporting period. Significant estimates include the recoverability and useful lives of long-lived assets, the fair value of the Company’s stock, stock-based compensation fair values relating to warrant and other derivative liabilities and the valuation allowance related to deferred tax assets. Actual results may differ from these estimates.


Revenue Recognition

The Company derives its revenue primarily from the sale of its medical device, the PURE EP™ System, and well as related support and maintenance services and software upgrades in connection with the system.

The Company recognizes revenue in accordance with Accounting Standards Codification (ASC) 606, Revenue from Contracts with Customers (“ASC 606”). The core principle of ASC 606 is that an entity recognizes revenue to depict

the transfer of promised goods or services to customers in an amount that reflects the consideration to which the entity expects to be entitled in exchange for those goods or services.

The Company determines revenue recognition through the following five steps:

Identify the contract with the customer;

Identify the performance obligations in the contract;

Determine the transaction price;

Allocate the transaction price to the performance obligation in the contract; and

Recognize revenue when, or as, the performance obligations are satisfied.

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2022

(unaudited)

Performance obligations are the unit of accounting for revenue recognition and generally represent the distinct goods or services that are promised to the customer. If the Company determines that it has not satisfied a performance obligation, it will defer recognition of the revenue until the performance obligation is deemed to be satisfied. Once the PURE EP system is delivered, installed, and accepted by the customer, our performance obligation is recognized. Support, maintenance, and software upgrades are performance obligations over a defined period and are recognized ratably over the contractual service period. Customers typically purchase these services with the initial sale of the PURE EP System and do not have the right to terminate their contracts unless we fail to perform material obligations.

The Company may execute more than one contract with a single customer. If so, it is evaluated whether the agreements were negotiated as a package with a single objective, whether the amount of consideration to be paid in one agreement depends on the price and/or performance of another agreement, or whether the goods or services promised in the agreements represent a single performance obligation. The conclusions reached can impact the allocation of the transaction price to each performance obligation and the timing of revenue recognition related to those arrangements.

The Company records accounts receivable for amounts invoiced to customers for which the Company has an unconditional right to consideration as provided under the contractual arrangement. Unbilled receivables, if any, include amounts related to the Company’s contractual right to consideration for completed performance obligations not yet invoiced. Deferred revenue includes payments received in advance of performance under the contract. Our unbilled receivables and deferred revenue are reported on an individual contract basis at the end of each reporting period. Unbilled receivables are classified as current or noncurrent based on the timing of when we expect to bill the customer. Deferred revenue is classified as current or noncurrent based on the timing of when we expect to recognize revenue.

The Company’s unconditional right to consideration for goods and services transferred to the customer is included in accounts receivable, net (if any) in the Company’s consolidated balance sheet.

A reconciliation of contract liabilities with customers for the six months ended June 30, 2022 and 2021, are presented below:

Six months ended June 30, 2022:

  

Balance at

December 31, 2021

(000’s)

  

Consideration Received

(000’s)

  

Recognized in Revenue

(000’s)

  

Balance at

June 30, 2022

(000’s)

 

Product revenue

 $-  $-  $-  $- 

Service revenue

  37   -   (16

)

  21 

Total

 $37  $-  $(16

)

 $21 

Six months ended June 30, 2021:

  

Balance at

December 31, 2020

(000’s)

  

Consideration Received

(000’s)

  

Recognized in Revenue

(000’s)

  

Balance at

June 30, 2021

(000’s)

 

Product revenue

 $-  $314  $(314

)

 $- 

Service revenue

  -   64   (11

)

  53 

Total

 $-  $378  $(325

)

 $53 

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2022

(unaudited)

The table below summarizes our deferred revenue as of June 30, 2022 and December 31, 2021:

  

June 30, 2022

(000’s)

  

December 31, 2021

(000’s)

 

Deferred revenue-current

 $21  $32 

Deferred revenue-noncurrent

  -   5 

Total deferred revenue

 $21  $37 

The Company had one customer which accounted for approximately 100% of their revenue in the three and six months ended June 30, 2022.

The Company had one customer which accounted for approximately 96% of our revenue in the three months ended June 30, 2021 and two customers which accounted for approximately 61% and 39% of our revenue in the six months ended June 30, 2021.

The Company utilized one contract manufacturer for the manufacture and supply of the PURE EP system for the three and six months ended June 30, 2022 and 2021.

Cost of Goods Sold

Cost of goods sold consists primarily of the delivered cost of our medical device(s) sold.

Allowance for Doubtful Accounts

The Company adjusts accounts receivable down to net realizable value with its allowance methodology. In determining the allowance for doubtful accounts for estimated losses, aged receivables are analyzed periodically by management. Each identified receivable is reviewed based upon historical collection experience, financial condition of the customer and the status of any open or unresolved issues with the customer preventing the payment thereof. Corrective action, if necessary, is taken by the Company to resolve open issues related to unpaid receivables. The allowance for doubtful accounts was $0 at June 30, 2022 and December 31, 2021. The Company believes that its reserve is adequate, however results may differ in future periods. For the three and six months ended June 30, 2022 and 2021, bad debt expense totaled $0.

Concentrations of Credit Risk

Financial instruments and related items, which potentially subject the Company to concentrations of credit risk, consist primarily of cash and cash equivalents. The Company places its cash and temporary cash investments with credit quality institutions. At times, such amounts may be in excess of the FDIC insurance limit. At June 30, 2022 and December 31, 2021, deposits in excess of FDIC limits were $4.6 million and $11.2 million, respectively.

Fair Value of Financial Instruments


Accounting Standards Codification subtopic 825-10, Financial Instruments (“ASC 825-10”) requires disclosure of the fair value of certain financial instruments. The carrying value of cash, and cash equivalents, accounts payable and accrued liabilities as reflected in the balance sheets, approximate fair value because of the short-term maturity of these instruments. All other significant financial assets, financial liabilities and equity instruments of the Company are either recognized or disclosed in the financial statements together with other information relevant for making a reasonable assessment of future cash flows, interest rate risk and credit risk. Where practicable the fair values of financial assets and financial liabilities have been determined and disclosed; otherwise only available information pertinent to fair value has been disclosed.

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2022

(unaudited)

The Company follows Accounting Standards Codification subtopic 820-10, Fair Value Measurements and Disclosures (“ASC 820-10”) and Accounting Standards Codification subtopicASC 825-10, Financial Instruments (“ASC 825-10”), which permits entities to choose to measure many financial instruments and certain other items at fair value.

Inventory

Derivative Instrument Liability

The inventory is comprised of raw materials and finished goods available for sale and are stated at the lower of cost or net realizable value using specific identification method for serial numbered inventory and first-in, first-out method for all other inventory for valuation. The inventory at June 30, 2022 and December 31, 2021, inventory was comprised of the following:


  

June 30, 2022

(000’s)

  

December 31, 2021

(000’s)

 

Raw materials

 $176  $- 

Finished goods

  1,850   1,881 

Total inventory

 $2,026  $1,881 

Prepaid Expenses and Vendor Deposits

Prepaid expenses and vendor deposits are comprised of prepaid insurance, operating expenses and other prepayments.

Leases

The Company accounts for derivative instrumentsdetermines if a contractual arrangement is a lease at inception. Operating leases are included in accordance with ASC 815, which establishes accountingoperating lease right-of-use (“ROU”) assets, current operating lease liabilities, and reporting standards for derivative instruments and hedging activities, including certain derivative instruments embedded in other financial instruments or contracts and requires recognition of all derivativesnoncurrent operating lease liabilities on the Company’s consolidated balance sheetsheet. The Company evaluates and classifies leases as operating or finance leases for financial reporting purposes. The classification evaluation begins at fair value, regardless of hedging relationship designation. Accountingthe commencement date and the lease term used in the evaluation includes the non-cancellable period for changes in fair valuewhich the Company has the right to use the underlying asset, together with renewal option periods when the exercise of the derivative instruments depends on whetherrenewal option is reasonably certain and failure to exercise such option which result in an economic penalty. All the derivatives qualifyCompany’s real estate leases are classified as hedge relationshipsoperating leases. ROU assets represent the Company’s right to use an underlying asset for the lease term and lease liabilities represent the typesCompany’s obligation to make lease payments arising from the lease. Operating lease ROU assets and liabilities are recognized at the commencement date of relationships designated arethe lease based on the exposures hedged. At Septemberpresent value of lease payments over the lease term.

The lease payments included in the present value are fixed lease payments. As most of the Company’s leases do not provide an implicit rate, the Company estimates its collateralized incremental borrowing rate, based on information available at the commencement date, in determining the present value of lease payments. The Company applies the portfolio approach in applying discount rates to its classes of leases. The operating lease ROU assets include any payments made before the commencement date. Lease expense for lease payments is recognized on a straight-line basis over the lease term. The Company does not currently have subleases. The Company does not currently have residual value guarantees or restrictive covenants in its leases.

Property and Equipment

Property and equipment are stated at cost and depreciated using the straight-line method over their estimated useful lives of 3 to 5 years. When retired or otherwise disposed, the related carrying value and accumulated depreciation are removed from the respective accounts and the net difference less any amount realized from disposition, is reflected in earnings.

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 20172022

(unaudited)

Impairment of Long-lived Assets

The Company recognizes an impairment of long-lived assets used in operations, other than goodwill, when events or circumstances indicate that the asset might be impaired and December 31, 2016, the estimated undiscounted cash flows to be generated by those assets over their remaining lives are less than the carrying amount of those items. The net carrying value of assets not recoverable is reduced to fair value, which is typically calculated using the discounted cash flow method. The Company did not haverecognize and record any derivative instruments that were designated as hedges.impairments of long-lived assets used in operations during the three and six months ended June 30, 2022 and 2021.


At September 30, 2017 and December 31, 2016, the Company had outstanding preferred stock and warrants that contained embedded derivatives. These embedded derivatives include certain conversion features and reset provisions. (See Note 6 and Note 7).

Research and development costsDevelopment Costs


The Company accounts for research and development costs in accordance with the Accounting Standards Codification subtopic 730-10, Research and Development (“ASC 730-10”). Under ASC 730-10, all research and development costs must be charged to expense as incurred. Accordingly, internal research and development costs are expensed as incurred. Third-party research and developments costs are expensed when the contracted work has been performed or as milestone results have been achieved. Company-sponsored research and development costs related to both present and future products are expensed in the period incurred. The Company incurred research and development expenses of $1,124,506$1.4 million and $3,802,149$3.0 million for the three and ninesix months ended SeptemberJune 30, 2017;2022; $1.7 million and $560,514 and $2,139,671$2.9 million for the three and ninesix months ended SeptemberJune 30, 2016,2021, respectively.



BIOSIG TECHNOLOGIES, INC.
NOTES TO THE CONDENSED FINANCIAL STATEMENTS
SEPTEMBER 30, 2017
(unaudited)

Net Earnings (Loss)Income (loss) Per Common Share


The Company computes earnings (loss) per share under Accounting Standards Codification subtopic 260-10, Earnings Per Share (“ASC 260-10”). Net loss per common share is computed by dividing net loss by the weighted average number of shares of common stock outstanding during the year.period. Diluted earnings per share, if presented, would include the dilution that would occur upon the exercise or conversion of all potentially dilutive securities into common stock using the “treasury stock” and/or “if converted” methods as applicable.

The computation of basic and diluted loss per share as of SeptemberJune 30, 20172022 and 20162021 excludes potentially dilutive securities when their inclusion would be anti-dilutive, or if their exercise prices were greater than the average market price of the common stock during the period.


Potentially dilutive securities excluded from the computation of basic and diluted net lossincome (loss) per share are as follows:

 
September 30,
2017
  
September 30,
2016
  

June 30, 2022

  

June 30, 2021

 
Series C convertible preferred stock  656,667   726,667   257,524   52,028 
Options to purchase common stock  6,829,421   8,090,190   5,023,484   4,004,622 
Warrants to purchase common stock  11,380,582   8,333,235   3,649,123   887,262 

Restricted stock units to acquire common stock

  111,250   292,250 
Totals  18,866,670   17,150,092   9,041,381   5,236,162 

Stock Based Compensation


The Company measures the cost of services received in exchange for an award of equity instruments based on the fair value of the award. For employees and directors, the fair value of the award isas measured on the grant date and for non-employees, the fair value of the award is generally re-measured on vesting dates and interim financial reporting dates until the service period is complete.date. The fair value amount is then recognized over the period during which services are required to be provided in exchange for the award, usually the vesting period.


BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2017, the Company had 6,829,421 options outstanding to purchase shares of common stock, of which 6,427,005 were vested.2022

(unaudited)


As of December 31, 2016, the Company had 8,245,190 options outstanding to purchase shares of common stock, of which 7,028,639 were vested.

Income Taxes


The Company follows Accounting Standards Codification subtopic 740-10, Income Taxes (“ASC 740-10”) for recording the provision for income taxes. Deferred tax assets and liabilities are computed based upon the difference between the financial statement and income tax basis of assets and liabilities using the enacted marginal tax rate applicable when the related asset or liability is expected to be realized or settled. Deferred income tax expenses or benefits are based on the changes in the asset or liability during each period. If available evidence suggests that it is more likely than not that some portion or all of the deferred tax assets will not be realized, a valuation allowance is required to reduce the deferred tax assets to the amount that is more likely than not to be realized. Future changes in such valuation allowance are included in the provision for deferred income taxes in the period of change. Deferred income taxes may arise from temporary differences resulting from income and expense items reported for financial accounting and tax purposes in different periods.


Patents, Net

Deferred taxes

The Company capitalizes certain initial asset costs in connection with patent applications including registration, documentation and other professional fees associated with the application. Patent costs incurred prior to the Company’s U.S. Food and Drug Administration (“FDA”) 510(k) application on March 28, 2018 were charged to research and development expense as incurred. Commencing upon first in-man trials on February 18 and 19, 2019, capitalized costs are classifiedamortized to expense using the straight-line method over the lesser of the legal patent term or the estimated life of the product of 20 years. During the three and six months ended June 30, 2022, the Company recorded amortization of $4,752 and $9,503; and $4,752 and $9,503 for the three and six months ended June 30, 2021 to current period operations, respectively.

Warranty

The Company generally warrants its products to be free from material defects and to conform to material specifications for a period of up to two (2) years. Warranty expense is estimated based primarily on historical experience and is reflected in the unaudited condensed consolidated financial statements.

Non-controlling Interest

The Company’s non-controlling interest represents the non-controlling shareholders ownership interests related to the Company’s subsidiary, ViralClear. The Company reports its non-controlling interest in subsidiaries as current or non-current, dependinga separate component of equity in the unaudited condensed consolidated balance sheets and reports both net loss attributable to the non-controlling interest and net loss attributable to the Company’s common shareholders on the classificationface of assetsthe unaudited condensed consolidated statements of operations. The Company’s equity interest in ViralClear is 69.08% and liabilitiesthe non-controlling stockholders’ interest is 30.92% as of June 30, 2022. This is reflected in the unaudited condensed consolidated statements of changes in equity.

Segment Information

Operating segments are identified as components of an enterprise about which separate discrete financial information is available for evaluation by the chief operating decision maker, or decision-making group, in making decisions how to which they relate.  Deferred taxes arising from temporary differences that are notallocate resources and assess performance. The information disclosed herein represents all of the material financial information related to the Company’s principal operating segments. (See Note 11 – Segment Reporting).

Recent Accounting Pronouncements

In June 2016, the FASB issued ASU 2016-13, Financial Instruments-Credit Losses (Topic 326): Measurement of Credit Losses on Financial Instruments (“ASU 2016-13”), which requires the measurement and recognition of expected credit losses for financial assets held at amortized cost. ASU 2016-13 replaces the existing incurred loss impairment model with an asset or liability are classifiedexpected loss model that requires the use of forward-looking information to calculate credit loss estimates. It also eliminates the concept of other-than-temporary impairment and requires credit losses on available-for-sale debt securities to be recorded through an allowance for credit losses instead of as current or non-current depending ona reduction in the amortized cost basis of the securities. ASU 2016-13 was effective for annual periods, and interim periods within those annual periods, beginning after December 15, 2019. Early adoption was permitted, including adoption in which the temporary differences are expected to reverse and are considered immaterial.any interim period.



BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

SEPTEMBER

JUNE 30, 20172022

(unaudited)

(unaudited)


Registration Rights

The Company accounts for registration rights agreements in accordance with

In February 2020, the FASB issued ASU 2020-02, Financial Instruments-Credit Losses (Topic 326) and Leases (Topic 842) - Amendments to SEC Paragraphs Pursuant to SEC Staff Accounting Standards Codification subtopic 825-20, Registration Payment Arraignments (“ASC 825-20”). Under ASC 825-20, the Company is requiredBulletin No. 119 and Update to disclose the nature and terms of the arraignment, the maximum potential amount andSEC Section on Effective Date Related to assess each reporting period the probable liability under these arraignments and, if exists, to record or adjust the liability to current period operations.  


Beginning on October 28, 2016, the Company entered into subscription agreements with certain accredited investors pursuant to which the Company sold to the investors units, which each unit consisting of one share of the Company’s common stock and a warrant to purchase one half of one share of common stock (the “Private Placement”).  In connection with the Private Placement, the Company also entered into a registration rights agreements with the investors, pursuant to which the Company agreed to provide certain registration rights with respect to the common stock and warrants issued under the Private Placement.  The registration rights agreements require the Company to file a registration statement within 45 calendar days upon the final closing under the Private Placement and to be effective 120 calendar days thereafter. The final closing under the Private Placement occurred on March 31, 2017. On June 8, 2017, the Company filed the required registration statement and on September 19, 2017 was declared effective. The Company has estimated the liability under the registration rights agreement at $-0- as of September 30, 2017.

Recent Accounting Pronouncements

In July 2017, the Financial Accounting Standards Board (“FASB”) issued Accounting Standards Update (“ASU”) No. 2017-11, Earnings Per Share (Topic 260)2016-02, Leases (Topic 842), Distinguishing Liabilities from Equity (Topic 480), Derivatives and Hedging (Topic 815). The amendments in Part I of this Update changewhich amended the classification analysis of certain equity-linked financial instruments (or embedded features) with down round features. When determining whether certain financial instruments should be classified as liabilities or equity instruments, a down round feature no longer precludes equity classification when assessing whether the instrument is indexed to an entity’s own stock. The amendments also clarify existing disclosure requirements for equity-classified instruments. As a result, a freestanding equity-linked financial instrument (or embedded conversion option) no longer would be accounted for as a derivative liability at fair value as a resulteffective date of the existence of a down round feature. For freestanding equity classified financial instruments, theoriginal pronouncement for smaller reporting companies. ASC 2016-13 and its amendments require entities that present earnings per share (EPS) in accordance with Topic 260 to recognize the effect of the down round feature when it is triggered. That effect is treated as a dividend and as a reduction of income available to common shareholders in basic EPS. Convertible instruments with embedded conversion options that have down round features are now subject to the specialized guidance for contingent beneficial conversion features (in Subtopic 470-20, Debt—Debt with Conversion and Other Options), including related EPS guidance (in Topic 260). The amendments in Part II of this Update recharacterize the indefinite deferral of certain provisions of Topic 480 that now are presented as pending content in the Codification, to a scope exception.

Those amendments do not have an accounting effect. For public business entities, the amendments in Part I of this Update arewill be effective for fiscal years,annual and interim periods within those fiscal years, beginning after December 15, 2018. Early adoption is permitted2022 for all entities, including adoption in an interim period. If an entity early adopts the amendments in an interim period, any adjustments should be reflected as of the beginning of the fiscal year that includes that interim period.smaller reporting companies. The Company anticipates earlydoes not expect to have a material impact on the Company’s financial position, results of operations or cash flows upon adoption of this pronouncement effective January 1, 2018.  As such, the impact would the reclassification of the December 31, 2017 fair values of our warrant and derivative liabilities to equity.new standard.


There arewere other various other updates recently issued, most of which represented technical corrections to the accounting literature or application to specific industries and are not expected to a have a material impact on the Company'sCompany’s financial position, results of operations or cash flows.


Subsequent Events

The Company evaluates events that have occurred after the balance sheet date but before the financial statements are issued.  Based upon the evaluation, the Company did not identify any recognized or non-recognized subsequent events that would have required adjustment or disclosure in the condensed financial statements, except as disclosed.


BIOSIG TECHNOLOGIES, INC.
NOTES TO THE CONDENSED FINANCIAL STATEMENTS
SEPTEMBER 30, 2017
(unaudited)

NOTE 4 PROPERTY AND EQUIPMENT

Property and equipment as of SeptemberJune 30, 20172022 and December 31, 20162021 is summarized as follows:

 
September 30,
2017
  
December 31,
2016
  

June 30, 2022

(000’s)

  

December 31, 2021

(000’s)

 
Computer equipment $85,549  $84,704  $392  $383 
Furniture and fixtures  11,837   10,117   88   88 
Subtotal  97,386   94,821 

Manufacturing equipment

  304   286 

Testing/Demo equipment

  178   145 

Leasehold improvements

  79   79 

Total

  1,041   981 
Less accumulated depreciation  (78,520)  (70,633)  (445

)

  (329

)

Property and equipment, net $18,866  $24,188  $596  $652 


During the nine months ended September 30, 2017, the Company distributed equipment with a book value of $3,210 to a prior employee in connection with a settlement agreement.

Property and equipment are stated at cost and depreciated using the straight-line method over their estimated useful lives of 3 to 5 years. Leasehold improvements are depreciated over the related expected lease term. When retired or otherwise disposed, the related carrying value and accumulated depreciation are removed from the respective accounts and the net difference less any amount realized from disposition, is reflected in earnings.

Depreciation expense was $2,834$66,243 and $8,900$116,625 for three and six months ended June 30, 2022 and $45,113 and $81,947 for the three and ninesix months ended SeptemberJune 30, 2017, respectively;2021, respectively

NOTE 5 RIGHT TO USE ASSETS AND LEASE LIABILITY

On April 4, 2022, the Company entered into a Seventh Amendment to the Office Lease at 12424 Wilshire Blvd in Los Angeles dated August 9, 2011 (the “Seventh Amendment”) – it is the Fifth Extended Term with respect to Suite 745 and $2,570the Expansion Term with respect to Suite 740 which is from July 1, 2022 until July 31, 2025 with a fixed monthly rent beginning at $14,124 and $7,811escalating yearly to $15,130 in the final year. The security deposit remains unchanged at $27,404.

The Company determined that the Seventh Amendment was a lease modification and accordingly reassessed the lease classification, remeasured the lease liability and adjusted the right-to-use asset. At April 4, 2022, the Company removed the remaining right-to-use net assets of $42,312 and related lease liability of $40,564 and recorded right-to-use assets and related lease liability of $502,445.

As of June 30, 2022 and December 31, 2021, the Company had outstanding 4 leases with aggregate payments of $32,143 per month, expiring through July 31, 2025.

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2022

(unaudited)

Right to use assets is summarized below:

  

June 30, 2022

(000’s)

  

December 31, 2021

(000’s)

 

Right to use asset

 $1,087  $803 

Less accumulated amortization

  (189

)

  (199

)

Right to use assets, net

 $898  $604 

During the three and six months ended June 30, 2022, the Company recorded $108,612 and $216,346 and $126,638 and $245,239 for the three and ninesix months ended SeptemberJune 30, 2016,2021 as lease expense to current period operations, respectively.


Lease liability is summarized below:

  

June 30, 2022

(000’s)

  

December 31, 2021

(000’s)

 

Total lease liability

 $950  $656 

Less: short term portion

  (341

)

  (283

)

Long term portion

 $609  $373 

Maturity analysis under these lease agreements are as follows (000’s):

Year ended December 31, 2022

 $181 

Year ended December 31, 2023

  393 

Year ended December 31, 2024

  370 

Year ended December 31, 2025

  106 

Total

  1,050 

Less: Present value discount

  (100

)

Lease liability

 $950 

Lease expense for the three months ended June 30, 2022 and 2021 was comprised of the following:

  

June 30, 2022

(000’s)

  

June 30, 2021

(000’s)

 

Operating lease expense

 $81  $119 

Short-term lease expense

  9   8 

Variable lease expense

  19   - 

Total

 $109  $127 

Lease expense for the six months ended June 30, 2022 and 2021 was comprised of the following:

  

June 30, 2022

(000’s)

  

June 30, 2021

(000’s)

 

Operating lease expense

 $166  $230 

Short-term lease expense

  18   15 

Variable lease expense

  32   - 

Total

 $216  $245 

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2022

(unaudited)

NOTE 56 ACCOUNTS PAYABLE AND ACCRUED EXPENSES

Accounts payable and accrued expenses at SeptemberJune 30, 20172022 and December 31, 20162021 consist of the following:

  
September 30,
2017
  
December 31,
2016
 
Accrued accounting and legal $165,424  $120,464 
Accrued reimbursements  12,222   43,116 
Accrued consulting  23,481   1,192 
Accrued research and development expenses  1,083,848   181,884 
Accrued office and other  1,992   10,202 
Deferred rent  1,303   2,912 
Accrued settlement related to arbitration  13,333   13,333 
  $1,301,603  $373,103 

NOTE 6 – SERIES C 9% CONVERTIBLE PREFERRED STOCK
On January 9, 2013, the Board of Directors authorized the issuance of up to 4,200 shares of 9% Series C Convertible Preferred Stock (the “Series C Preferred Stock”).

The Series C Preferred Stock is entitled to preference over holders of junior stock upon liquidation in the amount of $1,000 plus any accrued and unpaid dividends; entitled to dividends as a preference to holders of junior stock at a rate of 9% per annum of the stated value of $1,000 per share, payable quarterly beginning on September 30, 2013 and are cumulative.  The holders of the Series C Preferred Stock vote together with the holders of our common stock on an as-converted basis, but may not vote the Series C Preferred Stock in excess of the beneficial ownership limitation of the Series C Preferred Stock.  The beneficial ownership limitation is 4.99% of our then outstanding shares of common stock following such conversion or exercise, which may be increased to up to 9.99% of our then outstanding shares of common stock following such conversion or exercise upon the request of an individual holder.  The beneficial ownership limitation is determined on an individual holder basis, such that the as-converted number of shares of one holder is not included in the shares outstanding when calculating the limitation for a different holder.

11
  

June 30, 2022

(000’s)

  

December 31, 2021

(000’s)

 

Accrued accounting and legal

 $341  $204 

Accrued reimbursements and travel

  39   56 

Accrued consulting

  99   264 

Accrued research and development expenses

  162   367 

Accrued product purchases

  -   1 

Accrued marketing

  177   38 

Accrued office and other

  51   84 

Accrued payroll

  569   552 

Accrued settlement related to arbitration

  13   613 
  $1,451  $2,179 


BIOSIG TECHNOLOGIES, INC.
NOTES TO THE CONDENSED FINANCIAL STATEMENTS
SEPTEMBER 30, 2017
(unaudited)

In addition, absent the approval of holders representing at least 67% of the outstanding shares of the Series C Preferred Stock, we may not (i) increase the number of authorized shares of preferred stock, (ii) amend our charter documents, including the terms of the Series C Preferred Stock, in any manner adverse to the holders of the Series C Preferred Stock, including authorizing or creating any class of stock ranking senior to, or otherwise pari passu with, the shares of Series C Preferred Stock as to dividends, redemption or distribution of assets upon a liquidation, or (iii) perform certain covenants, including:

incur additional indebtedness;
permit liens on assets;
repay, repurchase or otherwise acquire more than a de minimis number of shares of capital stock;
pay cash dividends to our stockholders; and
engage in transactions with affiliates.

Any holder of Series C Preferred Stock is entitled at any time to convert any whole or partial number of shares of Series C Preferred Stock into shares of our common stock at a price of $1.50 per share. The Series C Preferred Stock is subject to full ratchet anti-dilution price protection upon the issuance of equity or equity-linked securities at an effective common stock purchase price of less than $1.50 per share as well as other customary anti-dilution protection.

In the event that:

  (i)  we fail to, or announce our intention not to, deliver common stock share certificates upon conversion of our Series C Preferred Stock prior to the seventh trading day after such shares are required to be delivered,
(ii)  we fail for any reason to pay in full the amount of cash due pursuant to our failure to deliver common stock share certificates upon conversion of our Series C Preferred Stock within five calendar days after notice therefor is delivered,
(iii)  we fail to have available a sufficient number of authorized and unreserved shares of common stock to issue upon a conversion of our Series C Preferred Stock,
 (iv)  we fail to observe or perform any other covenant, agreement or warranty contained in, or otherwise commit any breach of our obligations under, the securities purchase agreement, the registration rights agreement, the certificate of designation or the warrants entered into pursuant to the private placement transaction for our Series C Preferred Stock, which failure or breach could have a material adverse effect, and such failure or breach is not cured within 30 calendar days after written notice was delivered,
(v)  we are party to a change of control transaction,
(vi)  we file for bankruptcy or a similar arrangement or are adjudicated insolvent,
 (vii)  we are subject to a judgment, including an arbitration award against us, of greater than $100,000, and such judgment remains unvacated, unbonded or unstayed for a period of 45 calendar days,

The holders of the Series C Preferred Stock are entitled, among other rights, to redeem their shares of Series C Preferred Stock at any time for greater than their stated value or increase the dividend rate on their shares of Series C Preferred Stock to 18%.   The Company determined that certain of the defined triggering events were outside the Company’s control and therefore classified the Series C Preferred Stock outside of equity.
In connection with the sale of the Series C preferred stock, the Company issued an aggregate of 1,330,627 warrants to purchase the Company’s common stock at $2.61 per share expiring five years from the initial exercise date.  The warrants contain full ratchet anti-dilution price protection upon the issuance of equity or equity-linked securities at an effective common stock purchase price of less than $2.61 per share as well as other customary anti-dilution protection. The warrants are exercisable for cash; or if at any time after six months from the issuance date, there is no effective registration statement registering the resale, or no current prospectus available for the resale, of the shares of common stock underlying the warrants, the warrants may be exercised by means of a “cashless exercise”. 

As a result of an amendment to the conversion price of our Series C Preferred Stock, the full-ratchet anti-dilution protection provision of the warrants decreased the exercise price of the warrants from $2.61 per share to $1.50 per share and increased the aggregate number of shares issuable under the warrants to 2,315,301.

NOTE 7 STOCKHOLDERS EQUITY

12


BIOSIG TECHNOLOGIES, INC.
NOTES TO THE CONDENSED FINANCIAL STATEMENTS
SEPTEMBER 30, 2017
(unaudited)

In accordance with ASC 470-20, at issuance, the Company recognized an embedded beneficial conversion feature present in the Series C

Preferred Stock when it was issued. The Company allocated the net proceeds between the intrinsic value of the conversion option ($1,303,671) and the warrants ($1,064,739) to additional paid-in capital.  The aggregate debt discount, comprised of the relative intrinsic value of the conversion option ($1,303,671), the relative fair value of the warrants ($1,064,739), and the issuance costs ($412,590), for a total of $2,781,000, is amortized over an estimated one year as interest expense.


During the month of February 2013, the holders of previously issued convertible bridge notes converted into 600 shares of the Company’s Series C Preferred Stock.

During the months of February, March, May, and July 2013, the Company sold an aggregate of 2,181 shares of the Company’s Series C Preferred Stock for net proceeds of $1,814,910.

At the time of issuance and until March 31, 2015, the Company determined that the anti-dilutive provisions embedded in the Series C Preferred Stock and related issued warrants did not meet the defined criteria of a derivative in such that the net settlement requirement of delivery of common shares does not meet the “readily convertible to cash” as described in Accounting Standards Codification 815 and therefore bifurcation is not required.  There was no established market for the Company’s common stock.  As described in Note 7, as of March 31, 2015, the Company determined a market had been established for the Company’s common stock and accordingly, reclassified the fair value of the embedded reset provisions of the Series C Preferred Stock and warrants of $1,242,590 and $4,097,444, respectively, from equity to liabilities.
At March 31, 2015, the Company valued the reset provisions of the Series C Preferred Stock and warrants in accordance with ASC 470-20 using the Multinomial Lattice pricing model and the following assumptions: contractual terms of 2.78 to 3.50 years, a risk free interest rate of 0.56% to 0.89%, a dividend yield of 0%, and volatility of 141.00%.

During January 2015, the Company issued an aggregate of 42,334 shares of its common stock in exchange for 50 shares of the Company’s Series C Preferred Stock and accrued dividends.

During March 2015, the Company issued an aggregate of 169,334 shares of its common stock in exchange for 200 shares of the Company’s Series C Preferred Stock and accrued dividends.

In April 2015, the Company issued an aggregate of 152,401 shares of its common stock in exchange for 180 shares of the Company’s Series C Preferred Stock and accrued dividends.

On May 11, 2015, the Company sold an aggregate of 450 shares of its Series C Preferred Stock for net proceeds of $450,000.  In connection with the sale, the Company issued 374,641 warrants to purchase the Company’s common stock at an exercise price of $1.50 per share for five years with certain reset provisions as described above. The Company determined the initial fair values of the embedded beneficial conversion feature of the Series C Preferred Stock and the reset provisions of the related issued warrants $506,348 and $334,784, respectively, using a Multinomial Lattice pricing model and the following assumptions: estimated contractual terms of 2.00 years, a risk free interest rate of 0.25%, a dividend yield of 0%, and volatility of 140.00%.  The determined fair values were recorded as liabilities and a charge to current period operations.
In May 2015, the Company issued an aggregate of 273,473 shares of its common stock in exchange for 323 shares of the Company’s Series C Preferred Stock and accrued dividends.
In June 2015, the Company issued an aggregate of 296,333 shares of its common stock in exchange for 350 shares of the Company’s Series C Preferred Stock and accrued dividends.

In July 2015, the Company issued an aggregate of 169,333 shares of its common stock in exchange for 200 shares of the Company’s Series C Preferred Stock and accrued dividends.


BIOSIG TECHNOLOGIES, INC.
NOTES TO THE CONDENSED FINANCIAL STATEMENTS
SEPTEMBER 30, 2017
(unaudited)

In October 2015, the Company issued an aggregate of 143,935 shares of its common stock in exchange for 170 shares of the Company’s Series C Preferred Stock and accrued dividends.

In November 2015, the Company issued an aggregate of 99,061 shares of its common stock in exchange for 117 shares of the Company’s Series C Preferred Stock and accrued dividends.

In December 2015, the Company issued an aggregate of 84,667 shares of its common stock in exchange for 100 shares of the Company’s Series C Preferred Stock and accrued dividends.

In February 2016, the Company issued an aggregate of 54,859 shares of its common stock in exchange for 75 shares of the Company’s Series C Preferred Stock and accrued dividends.

In May 2016, the Company issued an aggregate of 197,713 shares of its common stock in exchange for 236 shares of the Company’s Series C Preferred Stock and accrued dividends.

In June 2016, the Company issued an aggregate of 54,759 shares of its common stock in exchange for 70 shares of the Company’s Series C Preferred Stock and accrued dividends.

In December 2016, the Company issued an aggregate of 18,188 shares of its common stock in exchange for 20 shares of the Company’s Series C Preferred Stock and accrued dividends.

In June 2017, the Company issued an aggregate of 60,846 shares of its common stock in exchange for 65 shares of the Company’s Series C Preferred Stock and accrued dividends.

In July 2017, the Company issued an aggregate of 19,844 shares of its common stock in exchange for 20 shares of the Company’s Series C Preferred Stock and accrued dividends.

Series C Preferred Stock issued and outstanding totaled 985 and 1,070 as of September 30, 2017 and December 31, 2016, respectively.  As of September 30, 2017 and December 31, 2016, the Company has accrued $396,939 and $359,891 dividends payable on the Series C Preferred Stock.

Registration Rights Agreement

In connection with the Company’s private placement of Series C Preferred Stock and warrants, the Company entered into a registration rights agreement with the purchasers pursuant to which the Company agreed to provide certain registration rights with respect to the common stock issuable upon conversion of Series C Preferred Stock and exercise of the warrants issued to holders of Series C Preferred Stock. Specifically, the Company agreed to file a registration statement with the Securities and Exchange Commission covering the resale of the common stock issuable upon conversion of the Series C Preferred Stock and exercise of the warrants on or before July 22, 2013 and to cause such registration statement to be declared effective by the Securities and Exchange Commission, in the event that the registration statement is not reviewed by the Securities and Exchange Commission, within five trading days after the Company is notified that registration statement is not being reviewed by the Securities and Exchange Commission, and by November 22, 2013 in the event that the registration statement is reviewed by the Securities and Exchange Commission and the Securities and Exchange Commission issues comments.

If (i) the registration statement is not filed by July 22, 2013, (ii) the registration statement is not declared effective by the Securities and Exchange Commission within five trading days after the Company is notified that the registration statement is not being reviewed by the Securities and Exchange Commission, in the case of a no review, (iii) the registration statement is not declared effective by the Securities and Exchange Commission by November 22, 2013 in the case of a review by the Securities and Exchange Commission pursuant to which the Securities and Exchange Commission issues comments or (iv) the registration statement ceases to remain continuously effective for more than 20 consecutive calendar days or more than an aggregate of 45 calendar days during any 12-month period after its first effective date, then the Company is subject to liquidated damage payments to the holders of the shares sold in the private placement in an amount equal to 0.25% of the aggregate purchase price paid by such purchasers per month of delinquency.


BIOSIG TECHNOLOGIES, INC.
NOTES TO THE CONDENSED FINANCIAL STATEMENTS
SEPTEMBER 30, 2017
(unaudited)

Notwithstanding the foregoing, (i) the maximum aggregate liquidated damages due under the registration rights agreement shall be 3% of the aggregate purchase price paid by the purchasers, and (ii) if any partial amount of liquidated damages remains unpaid for more than seven days, the Company shall pay interest of 18% per annum, accruing daily, on such unpaid amount.

Pursuant to the registration rights agreement, the Company must maintain the effectiveness of the registration statement from the effective date until the date on which all securities registered under the registration statement have been sold, or are otherwise able to be sold pursuant to Rule 144 without volume or manner-of-sale restrictions, subject to the right to suspend or defer the use of the registration statement in certain events.

The Company filed a registration statement on July 22, 2013, which was originally declared effective on June 23, 2014 and has subsequently filed required registration statements to maintain effectiveness.

NOTE 7 – WARRANT AND DERIVATIVE LIABILITIES

At the time of issuance and until March 31, 2015, the Company determined that the anti-dilutive provisions embedded in the Series C Preferred Stock and related warrants (see Note 6) did not meet the defined criteria of a derivative in such that the net settlement requirement of delivery of common shares does not meet the “readily convertible to cash” as described in Accounting Standards Codification 815 and therefore bifurcation was not required.  There was no established market for the Company’s common stock.   As of March 31, 2015, the Company determined a market had been established for the Company’s common stock and accordingly, reclassified from equity to liability treatment the fair value of the embedded reset provisions of the Series C Preferred Stock and warrants of $1,242,590 and $4,097,444, respectively.

The Company valued the reset provisions of the Series C Preferred Stock and warrants in accordance with ASC 470-20 using the Multinomial Lattice pricing model and the following assumptions: estimated contractual terms, a risk free interest rate of 0.56% to 0.89, a dividend yield of 0%, and volatility of 141.00%.
At September 30, 2017, the Company marked to market the fair value of the reset provisions of the Series C Preferred Stock and warrants and determined fair values of $285,032 and $2,240,510, respectively. The Company recorded a gain (loss) from change in fair value of derivatives of $113,724 and $(320,131) for the three and nine months ended September 30, 2017, respectively, and $17,771 and $(807,087) for the three and nine months ended September 30, 2016, respectively. The fair values of the embedded derivatives as of September 30, 2017 were determined using the Multinomial Lattice pricing model and the following assumptions: estimated contractual term of 0.25 to 2.61 years, a risk free interest rate of 1.05% to 1.47%, a dividend yield of 0%, and volatility of 150%.

NOTE 8 – STOCKHOLDER EQUITY

Preferred stock

The Company is authorized to issue 1,000,000 shares of $0.001 par value preferred stock. As of SeptemberJune 30, 20172022 and December 31, 2016,2021, the Company has authorizeddesignated 200 shares of Series A preferred stock, 600 shares of Series B preferred stock, and 4,200 shares of Series C Preferred Stock, 1,400 shares of Series D Preferred Stock, 1,000 shares of Series E Preferred Stock and 200,000 shares of Series F Preferred Stock. As of SeptemberJune 30, 20172022 and December 31, 2016,2021, there were 0 and 0 Series A and Series B preferred stock outstanding and 985 and 1,070no outstanding shares of Series CA, Series B, Series D, Series E and Series F preferred stock, respectively.stock.


In June 2017, the Company issued 60,846 shares of its common stock in exchange for 65 shares of the Company’s

Series C Preferred Stock

As of June 30, 2022 and accrued dividends.


In July 2017,December 31, 2021, the Company issued an aggregate of 19,844had 105 shares of its common stock in exchange for 20 shares of the Company’s Series C Preferred Stockstock issued and accrued dividends.

outstanding. During the six months ended June 30, 2022, the conversion price of the Series C Preferred stock was reset from $2.27 per share to $0.75 per share. As such, the Company recorded a noncash deemed dividend of $107,953 during the six months ended June 30, 2022.

15


BIOSIG TECHNOLOGIES, INC.
NOTES TO THE CONDENSED FINANCIAL STATEMENTS
SEPTEMBER 30, 2017
(unaudited)

Common stock


The Company is authorized to issue 200,000,000 shares of $0.001 par value common stock. As of SeptemberJune 30, 20172022 and December 31, 2016,2021, the Company had 26,413,74544,811,880 and 22,588,18435,567,180 shares issued and outstanding, respectively.


During the ninesix months ended SeptemberJune 30, 2017,2022, the Company issued 1,880,000 shares of common stock for services at a fair value of $2,083,500.

During the six months ended June 30, 2022, the Company issued an aggregate of 625,000 shares of its common stock for services totaling $894,749 ($1.43 per share).


During the nine months ended September 30, 2017, the Company entered into securities purchase agreements with investors pursuant to which the Company issued 2,870,865 shares of common stock and 1,615,964 warrants for aggregate proceeds of $4,120,904, net of $185,394 in expenses.

During the nine months ended September 30, 2017, the Company issued an aggregate of 135,000 and 124,75087,499 shares of its common stock for vested restricted stock unitsunits.

Sale of common stock

On March 21, 2022, the Company entered into a securities purchase agreement with several institutional and accredited investors, pursuant to which the Company sold in a registered direct offering an aggregate of 2,613,130 shares of the Company’s common stock, based compensation previously accrued in 2016.at an offering price of $1.15 per share and warrants to purchase up to 2,613,130 shares of common stock at an exercise price of $1.40 per share, that are exercisable six months after the date of issuance and will expire three and one-half years following the date of issuance, for gross proceeds of approximately $3.0 million, net of expenses of approximately $3,000.


In April 2017,
17

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2022

(unaudited)

On June 24, 2022, the Company entered into an underwriting agreement (the “Underwriting Agreement”) with Laidlaw & Company (UK) Ltd. (the “Underwriter”), which was amended and restated on June 28, 2022 (the “Amended and Restated Underwriting Agreement”), relating to a best-efforts public offering (the “June 2022 Offering”) of 4,341,667 shares of the Company’s common stock. The public offering price of the common stock was $0.75 per share. After the underwriting discounts, which includes a reduced discount with respect to certain Company-introduced investors, and offering expenses, the Company received net proceeds from the offering of approximately $2,818,000.

Pursuant to the Amended and canceled 10,744Restated Underwriting Agreement, the Company issued to the Underwriter, or its designees warrants to purchase up to an aggregate 217,083 shares of common stock, or 5% of the number of common stock sold in the offering. The underwriter warrants are exercisable following the date of issuance and ending five years from the date of the execution of the Underwriting Agreement, at a price per share equal to $0.90 per share (120% of the public offering price per share) and are exercisable on a “cashless” basis. The Company also agreed to reimburse the Underwriter for certain of their out-of-pocket expenses incurred in connection with the offering, including, among other things, the reasonable fees and expenses of counsel, which fees and expenses may not exceed $125,000.

ATM Sales Agreement

On May 17, 2022, the Company entered into an ATM Sales Agreement (the “Sales Agreement”) with Virtu Americas LLC to act as the Company’s sales agent or principal (“Agent”), with respect to the issuance and sale of up to $10.0 million of the Company’s shares of common stock, from time to time in an at-the-market public offering.

Upon delivery of a placement notice and subject to the terms and conditions of the Sales Agreement, Virtu Americas LLC may sell the common stock by any method permitted by law deemed to be an “at the market offering” as defined in Rule 415(a)(4) promulgated under the Securities Act of 1933, as amended. The Company may sell the common stock in amounts and at times to be determined by the Company from time to time subject to the terms and conditions of the Sales Agreement, but it has no obligation to sell any of the common stock under the Sales Agreement. The Company or Virtu Americas LLC may suspend or terminate the offering of common stock upon notice to the other party and subject to other conditions. Virtu Americas LLC will act as sales agent on a commercially reasonable efforts basis consistent with its normal trading and sales practices and applicable state and federal law, rules and regulations and the rules of Nasdaq.

The Company will pay Agent a commission of up to 3.0% of the gross proceeds from the sale of the common stock pursuant to the Sales Agreement.

The offering of common stock pursuant to the Sales Agreement will terminate upon the earlier of (i) the sale of all common stock subject to the Sales Agreement or (ii) termination of the Sales Agreement in accordance with its terms.

The common stock was sold and issued pursuant the Company’s shelf registration statement on Form S-3 (File No. 333-251859), which was previously declared effective by the Securities and Exchange Commission, and a related prospectus.

From May 19, 2022 through June 15, 2022, the Company sold 322,404 shares of its common stock as paymentthrough the Sales Agreement for short-swing profit pursuant to Section 16(b)net proceeds of the U.S. Securities Exchange Act$302,192, after transactional costs of 1934, as amended from an officer and member$46,065.


BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2022

(unaudited)

NOTE 98 OPTIONS, RESTRICTED STOCK UNITS AND WARRANTS


BioSig Technologies, Inc.

Options

2012 Equity Incentive Plan


On October 19, 2012, the Company’s Board of Directors of BioSig Technologies, Inc. approved the 2012 Equity Incentive Plan (“the “Plan)(the “Plan”) and terminated the Long-Term Incentive Plan (the “2011 Plan”). The Plan (as amended) provides for the issuance of options, stock appreciation rights, restricted stock and restricted stock units to purchase up to 15,186,123 (as amended)14,474,450 shares of the Company’s common stock to officers, directors, employees and consultants of the Company (as amended).Company. Under the terms of the Plan the Company may issue Incentive Stock Options as defined by the Internal Revenue Code to employees of the Company only and nonstatutory options. The Board of Directors of the Company or a committee thereof administers the Plan and determines the exercise price, vesting and expiration period of the grants under the Plan.


However, the exercise price of an Incentive Stock Option should not be less than 110% of fair value of the common stock at the date of the grant for a 10% or more stockholder and 100% of fair value for a grantee who is not 10% stockholder. The fair value of the common stock is determined based on the quoted market price or in absence of such quoted market price, by the administrator in good faith.

Additionally, the vesting period of the grants under the Plan will be determined by the administrator, in its sole discretion, with an expiration period of not more than ten years.


The following table presents information related to stock options at September 30, 2017:

Options Outstanding Options Exercisable 
    Weighted   
    Average Exercisable 
Exercise Number of Remaining Life Number of 
Price Options In Years Options 
$1.01-2.00   2,144,642   5.9   1,742,226 
 2.01-3.00   4,384,779   3.9   4,384,779 
 3.01-4.00   300,000   7.5   300,000 
     6,829,421   4.7   6,427,005 


BIOSIG TECHNOLOGIES, INC.
NOTES TO THE CONDENSED FINANCIAL STATEMENTS
SEPTEMBER 30, 2017
(unaudited)

A summaryawards under the terms of the stock option activity and related information for the 2012 Plan for the nine months ended September 30, 2017 is as follows:

        Weighted-Average    
     Weighted-Average  Remaining  Aggregate 
  Shares  Exercise Price  Contractual Term  Intrinsic Value 
Outstanding at December 31, 2016  8,245,190  $2.24   5.8  $- 
Grants  -       0  $- 
Exercised  -             
Canceled  (1,415,769)  2.17         
Outstanding at September 30, 2017  6,829,421  $2.26   4.7  $2,000 
Exercisable at September 30, 2017  6,427,005  $2.29   4.6  $1,363 

The aggregate intrinsic value in the preceding tables represents the total pretax intrinsic value, based on options with an exercise price less than the Company’s stock price of $1.36 as of SeptemberJune 30, 2017, which would have been received by the option holders had those option holders exercised their options as of that date.2022.


Options

Option valuation models require the input of highly subjective assumptions. The fair value of stock-based payment awards was estimated using the Black-Scholes option model with a volatility figure derived from an index of historical stock prices of comparable entities until sufficient data exists to estimate the volatility using the Company’s own historical stock prices. Management determined this assumption to be a more accurate indicator of value.Company. The Company accounts for the expected life of options using the based on the contractual life of options for non-employees.


For employees, the Company accounts for the expected life of options in accordance with the “simplified” method, which is used for “plain-vanilla” options, as defined in the accounting standards codification. The risk-free interest rate was determined from the implied yields of U.S. Treasury zero-coupon bonds with a remaining life consistent with the expected term of the options.  The fair value of stock-based payment awards during

During the ninesix months ended SeptemberJune 30, 20172022, the Company granted an aggregate of 1,185,000 options to officers, directors and 2016 was estimated using the Black-Scholes pricing model.key consultants.


The fair value of all options vesting during the three and nine months ended September 30, 2017 of $54,243 and $151,470, respectively and during the three and nine months ended September 30, 2016 of $218,085 and $2,512,886, respectively, was charged to current period operations.  Unrecognized compensation expense of $135,041 and $310,817 at September 30, 2017 and December 31, 2016, respectively, will be expensed in future periods.

Restricted Stock

The following table summarizes the restricted stock activity for the nine month ended September 30, 2017:

Total restricted shares issued as of December 31, 2016135,000
Granted-
Vested(135,000)
Vested restricted shares as of September 30, 2017-
Unvested restricted shares as of September 30, 2017-

Stock based compensation expensepresents information related to restricted stock grants was $2,380 and $93,262 for the three and nine months ended Septemberoptions at June 30, 2017; $70,753 and $124,139 for the three and nine months ended September 30, 2016.  As of September 30, 2017, the stock-based compensation relating to restricted stock of $0 remains unamortized.2022:


 

Options Outstanding

 

 

Options Exercisable

 

 

 

 

 

 

 

 

 

 

Weighted

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Average

 

 

Exercisable

 

 

Exercise

 

 

Number of

 

 

Remaining Life

 

 

Number of

 

 

Price

 

 

Options

 

 

In Years

 

 

Options

 

 

$

Under 1.00

 

 

 

155,000

 

 

 

9.9

 

 

 

50,000

 

  

1.00-1.99

   

1,030,000

   

9.7

   

32,500

 

 

 

2.00-2.99

 

 

 

975,375

 

 

 

8.4

 

 

 

549,375

 

 

 

3.00-3.99

 

 

 

462,466

 

 

 

4.4

 

 

 

404,132

 

 

 

4.00-4.99

 

 

 

1,467,916

 

 

 

5.2

 

 

 

1,163,607

 

 

 

5.00-5.99

 

 

 

156,132

 

 

 

6.6

 

 

 

128,628

 

 

 

6.00-6.99

 

 

 

396,542

 

 

 

5.0

 

 

 

359,352

 

 

 

7.00-7.99

 

 

 

186,720

 

 

 

5.3

 

 

 

178,387

 

 

 

Over 8.00

 

 

 

193,333

 

 

 

7.4

 

 

 

181,236

 

 

 

 

 

 

 

5,023,484

 

 

 

6.9

 

 

 

3,047,217

 


BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

SEPTEMBER

JUNE 30, 2017

(unaudited)
Warrants

The following table summarizes information with respect to outstanding warrants to purchase common stock of the Company at September 30, 2017:

Exercise  Number Expiration
Price  Outstanding Date
$0.001   383,320 January 2020
$1.50   7,258,936 February 2018 to September2020
$1.84   35,076 January 2020
$1.95   1,689,026 October 2018 to September 2019
$2.00   100,000 August 2018
$2.02   30,755 January 2020
$2.50   100,000 August 2018
$2.75   228,720 August 2019 to September 2019
$3.67   214,193 December 2018 to January 2019
$3.75   1,340,556 April 2019 to March 2020
     11,380,582  

On February 9, 2017, the Company exchanged 38,572 warrants with an exercise price of $2.10 with 45,001 warrants with an exercise price of $1.50, all other terms and conditions the same, to 2016 investors to adjust offered terms in connection with the Company’s equity raise with other investors.

On February 10, 2017, the Company issued an aggregate of 300,628 warrants to purchase the Company’s common stock at $1.50 per share, expiring on February 10, 2020, in connection with the sale of the Company’s common stock.

On March 10, 2017, the Company issued an aggregate of 197,159 warrants to purchase the Company’s common stock at $1.50 per share, expiring on March 10, 2020, in connection with the sale of the Company’s common stock.

On March 15, 2017, the Company issued 630,000 warrants to purchase the Company’s common stock at $1.50 per share, expiring on March 15, 2020, to Mayo Foundation in connection with a know-how licensing agreement (See Note 10). The fair value of the of the issued warrants of $543,927, determined using the Black-Scholes option model with an estimated volatility of 105.22%, risk free rate of 1.599%, dividend yield of -0- and fair value of the Company’s common stock of $1.37, was charged to current period operations as acquired research and development.

On March 31, 2017, the Company issued an aggregate of 157,250 warrants to purchase the Company’s common stock at $1.50 per share, expiring on March 31, 2020, in connection with the sale of the Company’s common stock.

On April 6, 2017, the Company issued an aggregate of 288,300 warrants to purchase the Company’s common stock at $1.50 per share, expiring on April 6, 2020, in connection with the sale of the Company’s common stock.

On May 5, 2017, the Company issued an aggregate of 6,667 warrants to purchase the Company’s common stock at $1.50 per share, expiring on May 5, 2020, in connection with the sale of the Company’s common stock.

On May 17, 2017, the Company issued an aggregate of 186,957 warrants to purchase the Company’s common stock at $1.50 per share, expiring on May 17, 2020, for placement agent services in connection with the sale of the Company’s common stock.

On June 20, 2017, the Company issued 10,000 warrants to purchase the Company’s common stock at $1.50 per share, expiring on June 20, 2020, in connection with the sale of the Company’s common stock.

2022

(unaudited)

18



BIOSIG TECHNOLOGIES, INC.
NOTES TO THE CONDENSED FINANCIAL STATEMENTS
SEPTEMBER 30, 2017
(unaudited)

On June 30, 2017, the Company issued an aggregate of 108,334 warrants to purchase the Company’s common stock at $1.50 per share, expiring on June 30, 2020, in connection with the sale of the Company’s common stock.

On July 13, 2017, the Company issued an aggregate of 133,501 warrants to purchase the Company’s common stock at $1.50 per share, expiring on July 13, 2020, in connection with the sale of the Company’s common stock.

On August 18, 2017, the Company issued an aggregate of 175,500 warrants to purchase the Company’s common stock at $1.50 per share, expiring on August 18, 2020, in connection with the sale of the Company’s common stock.

On September 18, 2017, the Company issued an aggregate of 51,668 warrants to purchase the Company’s common stock at $1.50 per share, expiring on September 18, 2020, in connection with the sale of the Company’s common stock.

Stock based compensation related to warrants issued for services was $0 for the three and nine months ended September 30, 2017 and $641 and $56,930 for the three and nine months ended September 30, 2016, respectively.

A summary of the warrantstock option activity and related information for the ninePlan for the six months ended SeptemberJune 30, 20172022 is as follows:


        Weighted-Average    
     Weighted-Average  Remaining  Aggregate 
  Shares  Exercise Price  Contractual Term  Intrinsic Value 
Outstanding at December 31, 2016  9,128,189  $1.96   2.1  $494,099 
Grants  2,290,965  $1.50   3.0   - 
Exercised  -             
Canceled  (38,572) $2.10   2.4   - 
Outstanding at September 30, 2017  11,380,582  $1.87   1.8  $563,097 
                 
Vested and expected to vest at September 30, 2017  11,380,582  $1.86   1.6  $520,932 
Exercisable at September 30, 2017  11,380,582  $1.86   1.6  $520,932 
          

Weighted-Average

     
      

Weighted-Average

  

Remaining

  

Aggregate

 
  

Shares

  

Exercise Price

  

Contractual Term

  

Intrinsic Value

 

Outstanding at December 31, 2021

  4,568,484  $4.57   6.9  $- 

Grants

  1,185,000  $1.23   10.0  $- 

Forfeited/expired

  (730,000

)

 $4.93         

Outstanding at June 30, 2022

  5,023,484  $3.72   6.9  $- 

Exercisable at June 30, 2022

  3,047,217  $4.65   5.6  $- 


The aggregate intrinsic value in the preceding tables represents the total pretax intrinsic value, based on warrantsoptions with an exercise price less than the Company’s stock price of $1.36BioSig Technologies, Inc. of $0.658 as of SeptemberJune 30, 2017,2022, which would have been received by the warrantoption holders had those warrantoption holders exercised their warrantsoptions as of that date.


On February 7, 2022, the Company granted an aggregate of 100,000 options to purchase the company’s common stock in connection with the services rendered at the exercise price of $1.72 per share for a term of ten years with vesting on the quarterly for one year.

On February 17, 2022, the Company granted an aggregate of 66,000 options to purchase the company’s common stock in connection with the services rendered at the exercise price of $1.58 per share for a term of ten years with one-third vesting on the one-year anniversary and two-thirds vesting quarterly thereafter beginning February 17, 2023 for two years.

On March 15, 2022, the Company granted an aggregate of 70,000 options to purchase the company’s common stock in connection with the services rendered at the exercise price of $1.28 per share for a term of ten years with one-third vesting on the one-year anniversary and two-thirds vesting quarterly thereafter beginning March 15, 2023 for two years.

On March 30, 2022, the Company granted 350,000 options to purchase the company’s common stock in connection with the services rendered at the exercise price of $1.30 per share for a term of ten years with one-third vesting on the one-year anniversary and two-thirds vesting quarterly thereafter beginning March 30, 2023 for two years.

On April 13, 2022, the Company granted an aggregate of 444,000 options to purchase the company’s common stock in connection with the services rendered at the exercise price of $1.14 per share for a term of ten years with one-third vesting on the one-year anniversary and two-thirds vesting quarterly thereafter beginning April 13, 2023 for two years.

On May 12, 2022, the Company granted 50,000 options to purchase the company’s common stock in connection with the addition of a new board member at the exercise price of $0.82 per share for a term of ten years with half vesting immediately and half vesting April 22, 2023.

On May 16, 2022, the Company granted 50,000 options to purchase the company’s common stock in connection with the addition of a new board member at the exercise price of $0.87 per share for a term of ten years with half vesting immediately and half vesting May 2, 2023.

On June 15, 2022, the Company granted an aggregate of 55,000 options to purchase the company’s common stock in connection with the services rendered at the exercise price of $0.89 per share for a term of ten years with one-third vesting on the one-year anniversary and two-thirds vesting quarterly thereafter beginning June 15, 2023 for two years.

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2022

(unaudited)

The following assumptions were used in determining the fair value of options during the six months ended June 30, 2022:

Risk-free interest rate

  1.17% - 3.39

%

Dividend yield

  0

%

Stock price volatility

  83.83% to 92.93

%

Expected life

 

5.5 to 10 years

 

Weighted average grant date fair value

 $0.86 

On March 16, 2022, in connection with the termination of a Company executive, the Company extended the life of 100,000 previously issued options from the contractual 90 days from termination of service to the earlier of the initial life or March 16, 2024. The change in estimated fair value of the modified options of $15,181 was charged to current period operations.

The following assumptions were used in determining the change in fair value of the modified options at March 16, 2022:

Risk-free interest rate

0.44% - 1.95

%

Dividend yield

0

%

Stock price volatility

83.86

%

Expected life

0.25 – 2 years

The fair value of all options vesting during the three and six months ended June 30, 2022 of $356,394 and $1,006,386 and $613,806 and $1,190,692 for the three and six months ended June 30, 2021, respectively, was charged to current period operations. Unrecognized compensation expense of $2,600,031 at June 30, 2022 which the Company expects to recognize over a weighted average period of 1.06 years.

Warrants

The following table summarizes information with respect to outstanding warrants to purchase common stock of BioSig Technologies, Inc. at June 30, 2022:

 

Exercise

  

Number

 

Expiration

 

Price

  

Outstanding

 

Date

 $0.90   217,083 

June 2027

 $1.40   2,613,130 

September 2025

 $4.80   250,000 

February 2025 to July 2026

 $6.16   568,910 

November 2027

      3,649,123  

On March 21, 2022, the Company issued warrants to purchase 2,613,130 shares of its common stock at an exercise price of $1.40 per share, that are exercisable six months after the date of issuance and will expire three and one-half years following the date of issuance in connection with the sale of the Company’s common stock.

On June 29, 2022, the Company issued warrants to purchase 217,083 shares of common stock at an exercise price of $0.90 per share and will expire five years following the date of the execution of the Underwriting Agreement in connection with the sale of common stock in the June 2022 Offering.

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2022

(unaudited)

A summary of the warrant activity for the six months ended June 30, 2022 is as follows:

 

 

Shares

 

 

Weighted-Average Exercise Price

 

 

Weighted-Average Remaining Contractual Term

 

 

Aggregate Intrinsic Value

 

Outstanding at December 31, 2021

 

 

818,910

 

 

$

5.74

 

 

 

5.3

 

 

$

-

 

Issued

 

 

2,830,213

 

 

$

1.36

 

 

 

3.4

 

 

 

-

 

Outstanding at June 30, 2022

 

 

3,649,123

 

 

$

2.35

 

 

 

3.7

 

 

$

-

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Vested and expected to vest at June 30, 2022

 

 

3,649,123

 

 

$

2.35

 

 

 

3.7

 

 

$

-

 

Exercisable at June 30, 2022

 

 

1,035,993

 

 

$

4.73

 

 

 

4.8

 

 

$

-

 

The aggregate intrinsic value in the preceding tables represents the total pretax intrinsic value, based on options with an exercise price less than the company’s stock price of $0.658 of June 30, 2022, which would have been received by the option holders had those option holders exercised their options as of that date.

Restricted Stock Units

The following table summarizes the restricted stock activity for the six months ended June 30, 2022:

Restricted shares issued as of December 31, 2021

141,250

Granted

87,500

Vested and issued

(87,499

)

Forfeited

(30,001

)

Vested restricted shares as of June 30, 2022

-

Unvested restricted shares as of June 30, 2022

111,250

On March 8, 2022, the Company granted an aggregate of 37,500 restricted stock units for services with 12,500 vesting upon achievement of certain performance conditions and 25,000 vesting quarterly for one year.

On May 6, 2022, the Company granted 50,000 restricted stock units for services vesting one year from the date of issuance.

Stock based compensation expense related to restricted stock grants was $71,787 and $141,541 for the three and six months ended June 30, 2022 and $610,995 and $710,115 for the three and six months ended June 30, 2021, respectively. As of June 30, 2022, the stock-based compensation relating to restricted stock of $154,125 remains unamortized.

ViralClear Pharmaceuticals, Inc.

2019 Long-Term Incentive Plan

On September 24, 2019, ViralClear’s Board of Directors approved the 2019 Long-Term Incentive Plan (as subsequently amended, the “ViralClear Plan”). The ViralClear Plan was approved by BioSig as ViralClear’s majority stockholder. The ViralClear Plan provides for the issuance of options, stock appreciation rights, restricted stock and restricted stock units to purchase up to 4,000,000 shares of ViralClear’s common stock to officers, directors, employees and consultants of the ViralClear. Under the terms of the ViralClear Plan, ViralClear may issue Incentive Stock Options as defined by the Internal Revenue Code to employees of ViralClear only and nonstatutory options. The Board of Directors of ViralClear or a committee thereof administers the ViralClear Plan and determines the exercise price, vesting and expiration period of the grants under the ViralClear Plan.

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2022

(unaudited)

However, the exercise price of an Incentive Stock Option should not be less than 110% of fair market value of the common stock at the date of the grant for a 10% or more stockholder and 100% of fair market value for a grantee who is not 10% stockholder. The fair market value of the common stock is determined based on the quoted market price or in absence of such quoted market price, by the administrator in good faith.

Additionally, the vesting period of the grants under the ViralClear Plan will be determined by the administrator, in its sole discretion, with an expiration period of not more than ten years. There are 2,415,074 shares remaining available for future issuance of awards under the terms of the ViralClear Plan.

ViralClear Options

The following table presents information related to stock options at June 30, 2022:

 

Options Outstanding

  

Options Exercisable

 
         

Weighted

     
         

Average

  

Exercisable

 
 

Exercise

  

Number of

  

Remaining Life

  

Number of

 
 

Price

  

Options

  

In Years

  

Options

 
 $5.00   125,000   0.5   91,664 

The fair value of the stock-based payment awards was estimated using the Black-Scholes option model with a volatility figure derived from an index of historical stock prices of comparable entities with the market value of stock price based on recent sales. The Company accounts for the expected life of options in accordance with the “simplified” method, which is used for “plain-vanilla” options, as defined in the accounting standards codification. The risk-free interest rate was determined from the implied yields of U.S. Treasury zero-coupon bonds with a remaining life consistent with the expected term of the options.

The fair value of all options vesting during the three and six months ended June 30, 2022 of $0 and $36,520 and $36,521 and $73,041 for the three and six months ended June 30, 2021, respectively, was charged to current period operations. Unrecognized compensation expense of $0 at June 30, 2022 will be expensed in future periods.

Warrants (ViralClear)

The following table presents information related to warrants (ViralClear) at June 30, 2022:

 

Exercise

  

Number

 

Expiration

 

Price

  

Outstanding

 

Date

 $5.00   473,772 

November 2027

  10.00   6,575 

May 2025

      480,347  

Restricted stock units (ViralClear)

The following table summarizes the restricted stock activity for the six months ended June 30, 2022:

Restricted shares outstanding at December 31, 2021:

1,318,679

Forfeited

(240,000

)

Total restricted shares outstanding at June 30, 2022:

1,078,679

Comprised of:

Vested restricted shares as of June 30, 2022

678,679

Unvested restricted shares as of June 30, 2022

400,000

Total

1,078,679

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2022

(unaudited)

Stock based compensation expense related to restricted stock unit grants of ViralClear was $(744,767) and $(1,101,163) for the three and six months ended June 30, 2022 and $391,881 and $421,032 for the three and six months ended June 30, 2021, respectively. As of June 30, 2022, the stock-based compensation relating to restricted stock of $87,210 remains unamortized.

NOTE 9 NON-CONTROLLING INTEREST

On November 7, 2018, the Company formed a subsidiary, now known as ViralClear, to pursue additional applications of the PURE EP™ signal processing technology outside of cardiac electrophysiology, and subsequently in 2020, was repurposed to develop merimepodib, a broad-spectrum anti-viral agent that showed potential for the treatment of COVID-19. Since late 2020, ViralClear has been realigned with its original objective of pursuing additional applications of the PURE EP™ signal processing technology outside of cardiac electrophysiology.

As of June 30, 2022 and December 31, 2021, the Company had a majority interest in ViralClear of 69.08% and 68.44%, respectively.

A reconciliation of the ViralClear Pharmaceuticals, Inc. non-controlling loss attributable to the Company:

Net profit attributable to the non-controlling interest for the three months ended June 30, 2022 (000’s):

Net income

 $137 

Average Non-controlling interest percentage of profit/losses

  31.3

%

Net income attributable to the non-controlling interest

 $43 

Net loss attributable to the non-controlling interest for the three months ended June 30, 2021 (000’s):

Net loss

 $(1,167

)

Average Non-controlling interest percentage of profit/losses

  30.0

%

Net loss attributable to the non-controlling interest

 $(350

)

Net loss attributable to the non-controlling interest for the six months ended June 30, 2022 (000’s):

Net loss

 $(185

)

Average Non-controlling interest percentage of profit/losses

  31.9

%

Net loss attributable to the non-controlling interest

 $(59

)

Net loss attributable to the non-controlling interest for the six months ended June 30, 2021 (000’s):

Net loss

 $(1,971

)

Average Non-controlling interest percentage of profit/losses

  29.9

%

Net loss attributable to the non-controlling interest

 $(590

)

The following table summarizes the changes in non-controlling interest for the six months ended June 30, 2022 (000’s):

Balance, December 31, 2021

 $219 

Allocation of equity to non-controlling interest due to subsidiary shares issued in settlement of debt to parent

  292 

Allocation of equity to non-controlling interest due to equity-based compensation issued

  (332

)

Net loss attributable to non-controlling interest

  (59

)

Balance, June 30, 2022

 $120 

BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2022

(unaudited)

NOTE 10 COMMITMENTS AND CONTINGENCIES


Licensing agreements

Master Services Agreement

On January 1, 2022, the Company entered into a master services agreement with Access Strategy Partners Incorporated (“ASPI”) whereby ASPI will provide commercial executives assigned with specific customer targets and develop sales and marketing plans that are mutually agreed to between ASPI and the Company and assist in their execution. The agreement expires two years from the effective date, with an addition one year extension option.

The Company is obligated to pay ASPI: i) a monthly service fee of $40,000 and ii) 10% commission on all New Account revenue, as defined, on a quarterly basis.

2017 Know-How License Agreement

On March 15, 2017, the Company entered into a know-how license agreement with Mayo Foundation for Medical Education and Research whereby the Company was granted an exclusive license, with the right to sublicense, certain know how and patent applications in the field of signal processing, physiologic recording, electrophysiology recording, electrophysiology software and autonomics to develop, make and offer for sale. The agreement expires in ten years from the effective date.


The Company is obligated to pay to Mayo Foundation a 1% or 2% royalty payment on net sales of licensed products, as defined.


Patent and Know-How License Agreement EP Software Agreement

In consideration,

On November 20, 2019, the Company issued 630,000 warrantsentered into a patent and know-how license agreement (the “EP Software Agreement”) with Mayo Foundation for Medical Education and Research (“Mayo”). The EP Software Agreement grants to acquirethe Company an exclusive worldwide license, with the right to sublicense, within the field of electrophysiology software and under certain patent rights as described in the EP Software Agreement (the “Patent Rights”), to make, have made, use, offer for sale, sell and import licensed products and a non-exclusive license to the Company to use the research and development information, materials, technical data, unpatented inventions, trade secrets, know-how and supportive information of Mayo to develop, make, have made, use, offer for sale, sell, and import licensed products. The EP Software Agreement will expire upon the later of either (a) the expiration of the Patent Rights or (b) the 10th anniversary of the date of the first commercial sale of a licensed product, unless earlier terminated by Mayo for the Company’s common stock atfailure to cure a material breach of the EP Software Agreement, the Company’s or a sublicensee’s commencement of any action or proceedings against Mayo or its affiliates other than for an exercise priceuncured material breach of $1.50, expiring on March 15, 2020.the EP Software Agreement by Mayo, or insolvency of the Company.


In connection with the EP Software Agreement, the Company agreed to make earned royalty payments to Mayo in connection with the Company’s sales of the licensed products to third parties and sublicense income received by the Company and to make milestone payments of up to $625,000 in aggregate.

Amended and Restated Patent and Know-How License Agreement Tools Agreement

On November 20, 2019, the Company entered into an amended and restated patent and know-how license agreement (the “Tools Agreement”) with Mayo. The Tools Agreement contains terms of license grant substantially identical to the EP Software Agreement, although it is for different patent rights and covers the field of electrophysiology systems. In June 2021, patent rights were issued (“Valid Claim”) as defined whereby the Company paid milestone one of $75,000 during the 2021 year.

In connection with the Tools Agreement, the Company agreed to pay Mayo an upfront consideration of $100,000. The Company also agreed to make earned royalty payments to Mayo in connection with the Company’s sales of the licensed products to third parties and sublicense income received by the Company and to make milestone payments of up to $550,000 in aggregate.


BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2022

(unaudited)

ViralClear Patent and Know-How License Agreement

SEPTEMBER 30, 2017

On November 20, 2019, the Company’s majority-owned subsidiary, ViralClear, entered into a patent and know-how license agreement (the “ViralClear Agreement”) with Mayo. The ViralClear Agreement contains terms of license grant substantially identical to the EP Software Agreement and the Tools Agreement, although it is for different patent rights and covers the field of stimulation and electroporation for hypotension/syncope management, renal and non-renal denervation for hypertension treatment, and for use in treatment of arrhythmias in the autonomic nervous system.

(unaudited)

In connection with the ViralClear Agreement, ViralClear agreed to make earned royalty payments to Mayo in connection with ViralClear’s sales of the licensed products to third parties and sublicense income received by the Company and to make milestone payments of up to $700,000 in aggregate. In June 2021, patent rights were issued (“Valid Claim”) as defined whereby the Company paid milestone one of $75,000 during the 2021 year.


Trek Therapeutics, PBC

NOTE 11 – FAIR VALUE MEASUREMENT

In the event of sublicensing, sale, transfer, assignment or similar transaction, ViralClear agreed to pay Trek 10% of the consideration received.


As part of the acquired assets, ViralClear received an assignment and licensing rights agreement from Trek with a third-party vendor regarding certain formulas and compounds usage. The agreement calls for milestone payments upon marketing authorization (as amended and defined with respect of product in a particular jurisdiction in the territory, the receipt of all approvals from the relevant regulatory authority necessary to market and sell such product in any such jurisdiction, excluding any pricing approval or reimbursement authorization) in any first and second country of $10 million and $5 million, respectively, in addition to 6% royalty payments.

Defined Contribution Plan

Effective January 1, 2019, the Company established a qualified defined contribution plan (the “401(k) Plan”) pursuant to Section 401(k) of the Code, whereby all eligible employees may participate. Participants may elect to defer a percentage of their annual pretax compensation to the 401(k) plan, subject to defined limitations. The Company adoptedis required to make contributions to the provisions401(k) Plan equal to 3 percent of Accounting Standards Codification subtopic 825-10, Financial Instruments (“ASC 825-10”). ASC 825-10 defines fair value aseach participant’s eligible compensation, subject to limitations under the price that would be received from selling an asset or paid to transfer a liability in an orderly transaction between market participants atCode. For the measurement date. When determining the fair value measurements for assetsthree and liabilities required or permitted to be recorded at fair value,six months ended June 30, 2022, the Company considerscharged operations $67,888 and $135,528 and $56,962 and $128,427 for the principalthree and six months ended June 30, 2021, respectively, for contributions under the 401(k) Plan.

Purchase commitments

As of June 30, 2022, the Company had aggregate purchase commitments of approximately $2,268,011 for future services or most advantageous market inproducts, some of which it would transactare subject to modification or cancellations.

Litigation

The Company is subject at times to other legal proceedings and considers assumptions that market participants would use when pricing the asset or liability, such as inherent risk, transfer restrictions, and risk of nonperformance. ASC 825-10 establishes a fair value hierarchy that requires an entity to maximize the use of observable inputs and minimize the use of unobservable inputs when measuring fair value. ASC 825-10 establishes three levels of inputs that may be used to measure fair value:


Level 1 – Quoted prices in active markets for identical assets or liabilities.

Level 2 – Observable inputs other than Level 1 prices such as quoted prices for similar assets or liabilities; quoted prices in markets with insufficient volume or infrequent transactions (less active markets); or model-derived valuations inclaims, which all significant inputs are observable or can be derived principally from or corroborated by observable market data for substantially the full term of the assets or liabilities.

Level 3 – Unobservable inputs to the valuation methodology that are significant to the measurement of fair value of assets or liabilities.

All items required to be recorded or measured on a recurring basis are based upon level 3 inputs.

To the extent that valuation is based on models or inputs that are less observable or unobservablearise in the market, the determinationordinary course of fair value requires more judgment. In certain cases, the inputs used to measure fair valueits business. Although occasional adverse decisions or settlements may fall into different levels of the fair value hierarchy. In such cases, for disclosure purposes, the level in the fair value hierarchy within which the fair value measurement is disclosed and is determined based on the lowest level input that is significant to the fair value measurement.

Upon adoption of ASC 825-10, there was no cumulative effect adjustment to beginning retained earnings and no impact on the financial statements.

The carrying value of the Company’s cash and cash equivalents, accounts payable and other current assets and liabilities approximate fair value because of their short-term maturity.

As of September 30, 2017 and December 31, 2016, the Company did not have any items that would be classified as level 1 or 2 disclosures.

The Company recognizes its derivative and warrant liabilities as level 3 and values its derivatives using the methods discussed in Note 7. Whileoccur, the Company believes that the final disposition of such matters should not have a material adverse effect on its valuation methods are appropriatefinancial position, results of operations or liquidity.

NOTE 11 SEGMENT REPORTING

In accordance with ASC 280-10, the Company reports segment information based on the “management” approach. The management approach designates the internal reporting used by management for making decisions and consistent with other market participants, it recognizes thatassessing performance as the use of different methodologies or assumptions to determine the fair value of certain financial instruments could result in a different estimate of fair value at the reporting date. The primary assumptions that would significantly affect the fair values using the methods discussed in Note 5 are that of volatility and market pricesource of the underlying common stock of the Company.Company’s reportable segments. The Company has 3 reportable segments: BioSig Technologies, Inc. (parent), NeuroClear Technologies, Inc. and ViralClear Pharmaceuticals, Inc.


As of September 30, 2017 and December 31, 2016, the Company did not have any derivative instruments that were designated as hedges.


BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

SEPTEMBER

JUNE 30, 20172022

(unaudited)

(unaudited)


The derivative and warrant liability as of September 30, 2017, in

Information concerning the amount of $285,032 and $2,240,510, respectively, has a level 3 classification.


The following table provides a summary of changes in fair valueoperations of the Company’s level 3 financial liabilitiesreportable segments is as follows:

  

Three Months Ended June 30, 2022

(000's)

  

Three Months Ended June 30, 2021

(000's)

  

Six Months Ended June 30, 2022

(000's)

  

Six Months Ended June 30, 2021

(000's)

 

Revenues (from external customers)

                

 BioSig

 $8  $207  $16  $325 

 ViralClear

  -   -   -   - 

 NeuroClear

  -   -   -   - 
  $8  $207  $16  $325 

  

Three Months Ended June 30, 2022

(000's)

  

Three Months Ended June 30, 2021

(000's)

  

Six Months Ended June 30, 2022

(000's)

  

Six Months Ended June 30, 2021

(000's)

 

Operating Expenses:

                

BioSig

 $5,862  $7,026  $13,611  $14,800 

ViralClear

  (137)  1,166   185   1,971 

NeuroClear

  (1)  4   1   4 
  $5,724  $8,196  $13,797  $16,775 

  

Three Months Ended June 30, 2022

(000's)

  

Three Months Ended June 30, 2021

(000's)

  

Six Months Ended June 30, 2022

(000's)

  

Six Months Ended June 30, 2021

(000's)

 

Loss from Operations

                

BioSig

 $(5,854) $(6,881) $(13,595) $(14,635)

ViralClear

  137   (1,166)  (185)  (1,971)

NeuroClear

  1   (4)  (1)  (4)
  $(5,716) $(8,051) $(13,781) $(16,610)

  

June 30, 2022

(000’s)

  

December 31, 2021

(000’s)

 

Total Assets

        

BioSig

 $8,754  $13,595 

ViralClear

  836   1,924 

NeuroClear

  -   - 
  $9,590  $15,519 

NOTE 12 RELATED PARTY TRANSACTIONS

Accrued expenses related primarily to travel reimbursements, director fees and accrued compensation due related parties as of SeptemberJune 30, 2017:2022 and December 31, 2021 was $104,026 and $86,208, respectively.


  
Warrant
Liability
  Derivative 
Balance, December 31, 2016 $1,937,234  $288,934 
Total (gains) losses        
Transfers out due to conversion of Series C Preferred Stock  -   (20,757)
Mark to market to September 30, 2017  303,276   16,855 
Balance, September 30, 2017 $2,240,510  $285,032 
Loss on change in warrant and derivative liabilities for the nine months ended September 30, 2017 $(303,276) $(16,855)

Fluctuations in

During the three and six months ended June 30, 2022 and 2021, the Company’s stock price are a primary driverChief Financial Officer guaranteed issued corporate credit cards for the changes in the derivative valuations during each reporting period. As the stock price increases for eachno consideration.


BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

JUNE 30, 2022

(unaudited)

NOTE 12 13 SUBSEQUENT EVENTS


Equity Transactions

Series D Preferred stock

On November 3, 2017,July 6, 2022, the Company filedissued 2,500 shares of its common stock for vested restricted stock units.

On July 15, 2022, the CertificateCompany granted 150,000 shares of Designationsrestricted common stock vesting in equal monthly installments over six months for services valued at $95,400.

Sales-type Lease

On July 1, 2022, the Series D Preferred Stock with the SecretaryCompany entered a lease for our Pure EP system at a rate of State$4,333 per month. The term of the State of Delaware.  Pursuantlease is for 30 months with an option provided to such Certificate of Designations, inextend for an addition one year. The lease also has an option to purchase at the eventend of the Company’s liquidation or winding uplease at the fair market value.

The Company determined the lease meets the criteria of its affairs,a sales-type lease whereby the holders of Preferred Shares will be entitled to a liquidation preferencepresent value of the stated value per Preferred Sharefuture expected revenue, cost of $1,500 (the “Stated Value”) plus any accrued but unpaid dividends or any other fees due the holder. A total of 1,400 shares were designated as Series D Preferred Stock.


A holder of Preferred Shares is entitled at any time to convert any whole or partial number of shares of Preferred Shares into shares of Common Stock determined by dividing the Stated Value of the Preferred Shares being converted by the conversion price of $1.50 per share (the “Conversion Price”).  The Conversion Price is subject to “full ratchet” anti-dilution price protection upon the issuance of equity or equity-linked securities at a price lower than the Conversion Price as well as other customary anti-dilution protection.

A holder of the Preferred Shares shall be entitled to receive cumulative dividendssales and profit and loss are recognized at the rate per Preferred Share (as a percentage of the Stated Value per Preferred Share) of 9% per annum, with respect to the Series D Preferred Stock on each date that such Holder converts Preferred Shares into common stock (with respect only to Preferred Shares being converted).  The Company may pay such dividends, at its option, in cash, common stock or a combination thereof.  Payment of dividends in shares of common stock is subject to the satisfaction of certain equity conditions set forth in the Certificate of Designations.  Upon the conversion of Preferred Shares prior to November 3, 2020, the Company shall also pay to the Holders of the Preferred Shares so converted cash, or at the Company’s option, common stock or a combination thereof, with respect to the Preferred Shares so converted in an amount equal to $270 per $1,000 of Stated Value of the Preferred Shares being converted, less the amount of all prior dividends paid on such converted Preferred Shares before the relevant date of conversion.lease inception.



BIOSIG TECHNOLOGIES, INC.

NOTES TO THE CONDENSED FINANCIAL STATEMENTS
SEPTEMBER 30, 2017
(unaudited)

Preferred stock

On November 3, 2017,  the Company entered into a Securities Purchase Agreement (the “Purchase Agreement”) with certain institutional accredited investors (the “Investors”), pursuant to which the Company sold to the Investors an aggregate of 1,334 shares (the “Preferred Shares”) of its Series D Preferred Stock, par value $0.001 per share, and Class A Warrants to purchase an aggregate of 667,000 shares of the Company’s common stock, par value $0.001 per share at an exercise price of $1.75 per share (the “Class A Warrants”), in exchange for aggregate net cash proceeds of $1,929,975, net of expenses of $70,025. Contemporaneously with the entry into the Purchase Agreement, the Company and the Purchasers agreed to exchange outstanding warrants to purchase 780,506 shares of the Common Stock at an exercise price of $1.50 per share for new Class B Warrants to purchase an equal number of shares of common stock at the same exercise price (the “Class B Warrants”).

The Purchase Agreement contains representations and warranties of the Company and the Investors that are typical for transactions of this type.  The Purchase Agreement also contains covenants on the part of the Company that are typical for transactions of this type, as well as a prohibition on the Company’s ability to enter into equity line financings or other variable rate transactions.

In connection with the entry into the Purchase Agreement, the Investors and the Company also entered into a registration rights agreement whereby the Company agreed to file a registration statement with the Securities and Exchange Commission (the “SEC”) within 45 days of the closing of the transactions contemplated by the Purchase Agreement (the “Filing Date”) covering the resale of (a) all shares of Common Stock Issuable upon conversion of the Preferred Shares, (b) all shares of Common Stock issuable upon exercise of the Class A Warrants and Class B Warrants (the “Warrants”), (c) any additional shares of Common Stock issuable in connection with any anti-dilution provisions in the Warrants, and (d) any securities issued or then issuable upon any stock split, dividend or other distribution, recapitalization or similar event (“Registrable Securities”), not then registered.  The Company will use its reasonable best efforts to cause such registration statement to be declared effective by the SEC (such date, the “Effectiveness Date”) within 90 days of the Filing Date.

If (i) the registration statement is not filed on or prior to the Filing Date, (ii) the Company fails to file with the SEC a request for acceleration of a registration statement within 5 calendar days of the date that the Company is notified by the SEC that such registration statement will not be reviewed or will not be subject to further review, (iii) prior to the effective date of a registration statement, the Company fails to file a pre-effective amendment and otherwise respond in writing to comments made by the SEC in respect of such registration statement within 30 days after the receipt of comments by or notice from the SEC that such amendment is required in order for such registration statement to be declared effective, (iv) the registration statement is not declared effective by the Effectiveness Date or (v) certain other events described in the registration rights agreement (each, an “Event”), then the Company shall pay liquidated damages to the Investors in an amount equal to 1% of the aggregate purchase price paid by the Investors on the day of delinquency and each 30th day of delinquency thereafter.  Notwithstanding the foregoing, (i) the maximum aggregate liquidated damages due under the Registration Rights Agreement shall be 10% of the aggregate purchase price paid by the Investors.

Class A Warrants are exercisable immediately and expire on May 3, 2021, and have an exercise price of $1.75 per share.  The Class B Warrants are exercisable immediately and expire on November 3, 2020, and have an exercise price of $1.50.  The Class A Warrants and Class B Warrants otherwise have similar terms, including, a “full ratchet” anti-dilution adjustment in the event that the Company issues any common stock at a per share price lower than the applicable exercise price then in effect.


BIOSIG TECHNOLOGIES, INC.
NOTES TO THE CONDENSED FINANCIAL STATEMENTS
SEPTEMBER 30, 2017
(unaudited)

Common stock

On October 11, 2017, the Company entered into securities purchase agreements with investors, pursuant to which the Company received from subscriptions for the purchase of 386,667 shares of the Company’s common stock and warrants to purchase 193,334 shares of our common stock at $1.50, expiring three years from issuance, for aggregate net cash proceeds of $579,760, net of expenses of $140 (of which $279,940 were received as common stock subscriptions as of September 30, 2017). The shares of common stock were issued on October 11, 2017.

On October 25, 2017, the company granted awards to key employees, key consultants, and outside directors of 1,100,000 shares of restricted common stock; and incentive options to purchase 675,000 shares of common stock with a date of grant that is ten trading days following the date hereof and an exercise price equal to the arithmetic mean of the market price for such common stock for the ten trading days immediately preceding the grant date.

On November 6, 2017, the Company entered into securities purchase agreements with investors, pursuant to which the Company received from subscriptions for the purchase of 413,336 shares of the Company’s common stock and warrants to purchase 200,001 shares of our common stock at $1.50, expiring three years from issuance, for aggregate net cash proceeds of $619,830, net of expenses of $171.



ITEM 2. MANAGEMENT’SMANAGEMENTS DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS

This Management’sManagements Discussion and Analysis of Financial Condition and Results of Operations includes a number of forward-looking statements that reflect Management’sManagements current views with respect to future events and financial performance. You can identify these statements by forward-looking words such as “may,may, “will,will, “expect,expect, “anticipate,anticipate, “believe,believe, “estimate”estimate and “continue,continue, or similar words. Those statements include statements regarding the intent, belief or current expectations of us and members of our management team as well as the assumptions on which such statements are based. Prospective investors are cautioned that any such forward-looking statements are not guarantees of future performance and involve risk and uncertainties, and that actual results may differ materially from those contemplated by such forward-looking statements.

Readers are urged to carefully review and consider the various disclosures made by us in this report and in our other reports filed with the Securities and Exchange Commission. Important factors currently known to Management could cause actual results to differ materially from those in forward-looking statements. We undertake no obligation to update or revise forward-looking statements to reflect changed assumptions, the occurrence of unanticipated events or changes in the future operating results over time. We believe that our assumptions are based upon reasonable data derived from and known about our business and operations. No assurances are made that actual results of operations or the results of our future activities will not differ materially from our assumptions. Factors that could cause differences include, but are not limited to, expected market demand for our products, fluctuations in pricing for materials, and competition.

Business Overview


BioSig Technologies, Inc.

We are a development stage medical devicetechnology company that is developingcommercializing our PURE EP™ System which is an advanced signal acquisition and processing platform designed to provide essential diagnostic signals with high clinical value in all types of cardiac catheter ablations. PURE EP™ is designed to address long-standing limitations that slow and disrupt cardiac catheter ablation procedures, such as environmental lab noise, signal saturation, slow signal recovery, and inaccurate display of fractionated potentials.

Cardiac catheter ablation is a proprietary technologyprocedure that involves delivery of energy through the tip of a catheter that scars or destroys heart tissue to correct heart rhythm disturbances (arrhythmias). In August 2018, we received 510(k) clearance from the U.S. Food and Drug Administration (the “FDA”) to market our PURE (Precise Uninterrupted Real-time evaluation of Electrograms) EP™ System.

PURE EP™ is a signal processing platform that combines advanced hardware and software to address known challenges associated to signal acquisition, to enable electrophysiologists to see more signals and analyze them in real-time.The device aims to minimize noise and artifacts from cardiac recordings during electrophysiology studies and ablation. We are developing the PURE (Precise Uninterrupted Real-time evaluationacquire high-fidelity cardiac signals. Improving fidelity of Electrograms) EP System, a surface electrocardiogram and intracardiac multichannel recording and analysis system that acquires, processes and displays electrocardiogram and electrograms required during electrophysiology studies and ablation procedures.


The PURE EP System is designed to assist electrophysiologists in making clinical decisions in real-time by providing information that, we believe, is not always easily obtained, if at all, from any other equipment presently used in electrophysiology labs. The PURE EP System’s ability to acquire high fidelityacquired cardiac signals willmay potentially increase these signals’the diagnostic value and therefore offer improvedof these signals, thereby possibly improving accuracy and efficiency of the electrophysiologyEP studies and relatedablation procedures. We are developing

PURE EP™’s initial focus is on improving intracardiac signal processing tools withinacquisition and enhancing diagnostic information for catheter ablation procedures for complex arrhythmias like ventricular tachycardia (“VT”), a potentially life-threatening arrhythmia, and atrial fibrillation (“AF”), the most common cardiac arrhythmia associated with a fivefold risk of stroke.

Clinical data acquired by the PURE EP System. We believe that these will assist electrophysiologistsEP™ System in further differentiating true signals from noise, and will provide guidance in identifying ablation targets.

Since June 2011, we have collaborated with physicians affiliated with thea multi-center study at Texas Cardiac Arrhythmia Institute at St. David’s Medical Center in Austin, Texas, for initial technology validation. The physicians affiliated with the Texas Cardiac Arrhythmia Institute have provided us with digital recordings obtained with conventional electrophysiology recording systems during different stages of electrophysiology studies. Using our proprietary signal processing tools that are part of the PURE EP System, we analyzed these recordingsMayo Clinic in Jacksonville, Florida, and successfully removed baseline wander, noise and artifacts from the data thereby providing better diagnostic quality signals.
We are focused on improving the quality of cardiac recordings obtained during ablation of atrial fibrillation, the most common cardiac arrhythmia, and ventricular tachycardia, an arrhythmia evidenced by a fast heart rhythm originating from the lower chambers of the heart, which can be life-threatening. Cardiac ablation is a procedure that corrects conduction of electrical impulsesMassachusetts General Hospital in Boston, Massachusetts was published in September 2021 in the heart that cause arrhythmias. During this invasive procedure,Journal of Cardiovascular Electrophysiology and is available electronically with open access via the Wiley Online Library. Study results showed 93% consensus across the blinded reviewers with a catheter is usually inserted using a venous access into a specific area75% overall improvement in intracardiac signal quality and confidence in interpreting PURE EP™ signals over conventional sources. AF accounted for over 40% of the heart. A special radiofrequency generator delivers energy through the catheter to small areas of the heart muscle that cause the abnormal heart rhythm.enrollments.



According

We continue to install PURE EP™ Systems at centers of excellence for clinical evaluation under our market development plan. The PURE EP™ System has been utilized at numerous institutions, including Mayo Clinic campuses in Arizona, Florida and Minnesota; the University of Pennsylvania Hospital in Philadelphia, Pennsylvania; Overland Park Regional Medical System in Overland Park, Kansas; Deborah Heart and Lung Center in Browns Mills, New Jersey; St. Elizabeth’s Medical Center in Boston, Massachusetts; Medical City Heart Hospital in Dallas, Texas; Beth Israel Deaconess Medical Center (BIDMC) in Boston, Massachusetts, a 2009 articleteaching hospital of Harvard Medical School; Methodist Hospital in Circulation: ArrhythmiaSan Antonio, Texas; Houston Methodist Hospital; Medical City North Hills in North Richland Hills; Cleveland Clinic; and Electrophysiology, ablation is superior to pharmacological treatments and is becoming a first line of therapy for certain patientsWestside Regional Medical Center in Plantation, Florida.

To date, more than 2,500 patient procedures have been conducted with arrhythmias (“Treatment of Atrial Fibrillation With Antiarrhythmic Drugs or Radiofrequency Ablation,” Circulation: Arrhythmia and Electrophysiology (2009) 2: 349-361).


Our overall goal is to establish our proprietary technology as a new platform that will have the following advantages over the electrophysiology recording systems currently available on the market:
Higher quality cardiac signal acquisition for accurate and more efficient electrophysiology studies;
Precise, uninterrupted, real time evaluations of electrograms;
Reliable cardiac recordings to better determine precise ablation targets, strategy and end point of procedures; and
A portable device that can be fully integrated into existing electrophysiology lab environments.
If we are able to develop our product as designed, we believe that the PURE EPEP™ System and its signal processing tools will contribute to an increaseby more than 75 electrophysiologists across seventeen different clinical sites in the number of procedures performed in each electrophysiology lab and possibly improved patient outcomes.United States.

Our significant scientific achievements

In addition to date include:

Initial system concept validation was performed in collaboration with physicians at the Texas Cardiac Arrhythmia Institute at St. David’s Medical Center in Austin, Texas in June 2011. The Texas Cardiac Arrhythmia Institute provided challenging recordings obtained with electrophysiology recording systems presently in use at the institute during various electrophysiology studies. Our technology team successfully imported the data into the PURE EP System software and using proprietary signal processing, the PURE EP System software was able to reduce baseline wander, noise, and artifacts from the data and therefore provide better diagnostic quality signals.

Weclinical evaluation, we have established clinical and/or advisory relationships for both technology development and validation studies with physicians and researchers affiliated with the following medical centers: Texas Cardiac Arrhythmia Institute, Austin, TX; Cardiac Arrhythmia Center at the University of California at Los Angeles, Los Angeles, CA; Mount Sinai Medical Center, New York, NY; University Hospitals Case Medical Center, Cleveland, OH; Bringham & Women’s Hospital in Boston, MA; and Mayo Clinic, Rochester, MN.
The Cardiac Arrhythmia Center at the University of California at Los Angeles and Dr. Kalyanam Shivkumar, a former member of our board of directors, have played a significant role in the initial functional testing of our hardware. Dr. Shivkumar and his team have enabled us to learn the connectivity of the lab and its devices that pertain to where our PURE EP System will fit in. In June 2013, we commenced our first proof of concept pre-clinical study with the assistance of Dr. Shivkumar in order to further test the components of the PURE EP System hardware, as further explained below.
We are developing signal processing tools within the PURE EP System that will assist electrophysiologists in further differentiating true signals from noise, which may potentially provide guidance in identifying ablation targets. The signal processing tools are expected to be an integral part of the software of the PURE EP System, which we believe will significantly facilitate the locating of ablation targets.

In the second and third quarters of 2013, we performed and finalized testing of our proof of concept unit by initially using an electrocardiogram/intracardiac simulator at our lab, and subsequently by obtaining pre-clinical recordings from the lab at the University of California at Los Angeles. As part of the testing, we simultaneously recorded electrocardiogram and intracardiac signals on our proof of concept unit and GE’s CardioLab recording system. An identical signal was applied to the input of both systems and the monitor of our proof of concept unit was positioned next to the monitor of GE’s CardioLab recording system to allow for visual comparison. We believe that our proof of concept unit performed well as compared to GE’s CardioLab recording system, in that the electrocardiogram and intracardiac signals displayed on our proof of concept unit showed less baseline wander, noise and artifacts compared to signals displayed on GE’s CardioLab recording system. However, because this was a proof of concept test, without any clearly established protocols, we cannot present this data for publication and we do not have any independent verification or peer review of these findings.

In the third quarter of 2013, we analyzed the results of our proof of concept unit to determine the final design of the PURE EP System prototype, which has since been completed.
In September 2014, we performed additional tests on the PURE EP System prototype at the University of California at Los Angeles.
In the fourth quarter of 2014, we appointed Dr. Samuel J. Asirvatham from Mayo Clinic as a member of our Scientific Advisory Board and initiated plans for pre-clinical studies at Mayo Clinic.
In the first quarter of 2015, we appointed Dr. K. L. Venkatachalam from Mayo Clinic as a member of our Scientific Advisory Board. On March 31, 2015 Drs. Asirvatham and Venkatachalam performed our first pre-clinical study at Mayo Clinic in Rochester, Minnesota.
On June 10, 2015, Dr. Asirvatham performed our second pre-clinical study at Mayo Clinic in Rochester, Minnesota.
On November 17, 2015, Dr. Asirvatham performed our third pre-clinical study at Mayo Clinic in Rochester, Minnesota.
On February 22, 2016, we signed an agreement to initiate development of its PURE EP System with Minnetronix, Inc. (“Minnetronix”) and are taking steps toward its 510(k) submission.

On March 28, 2016, we announced an Advanced Research Program with Dr. Asirvatham at Mayo Clinic beginning June 2016.

On March 8, 2016, Dr. Ammar Killu from Mayo Clinic presented our preclinical data at the 13th Annual Dead Sea Symposium on Innovations in Cardiac Arrhythmias and Device Therapy in Tel Aviv, Israel entitled “Enhanced Electrophysiology Recording Improves Signal Acquisition and Differentiation”.

On June 2, 2016, Dr. Asirvatham performed our fourth pre-clinical study at Mayo Clinic in Rochester, Minnesota.

On June 23 and August 25 and 26, 2016, Dr. Vivek Reddy performed a pre-clinical study on a ventricular scar model at the Mount Sinai Hospital in New York, NY.

On July 27, 2016, Dr. Asirvatham performed our fifth pre-clinical study at Mayo Clinic in Rochester, Minnesota.

On September 14, 2016, Dr. Asirvatham performed our sixth pre-clinical study at Mayo Clinic in Rochester, Minnesota.

On August 19, 2016, we presented a poster at the IEEE Engineering in Medicine and Biology Society annual conference (IEEE EMBC 2016) entitled “Enhanced Electrophysiology Recording System”.

In December 2016, the Journal of the American College of Cardiology (JACC): Clinical Electrophysiology (Vol.2, No.7, pp.850) published  the article entitled, “Novel Electrophysiology Signal Recording System Enables Specific Visualization of the Purkinje Network and Other High-Frequency Signals”, submitted  by the Mayo Clinic team.

 ●On December 9, 2016, we filed a provisional patent application entitled “Assessment of Catheter Position by Local Electrogram”.

On December 9, 2016, we filed a provisional patent application entitled “Visualization of Conduction Tissue Signals”.
On February 14, 2017, Dr. Asirvatham performed our seventh pre-clinical study at Mayo Clinic in Rochester, Minnesota.
On March 15, 2017, Dr. Asirvatham performed our eighth pre-clinical study at Mayo Clinic in Rochester, Minnesota.
In April 2017, the PURE EP System was featured in The Journal of Innovations in Cardiac Rhythm Management with the manuscript entitled, “Initial Experience with the BioSig PURE EP™ Signal Recording System: An Animal Laboratory Experience” co-authored by physicians from Mayo Clinic and Harvard Brigham & Women’s Hospital.



On May 2, 2017, Dr. Asirvatham performed our ninth pre-clinical study at Mayo Clinic in Rochester, Minnesota.
On May 11, 2017, the PURE EP System was featured in a poster presentation at the Heart Rhythm Society’s 38th Annual Scientific Sessions entitled, “Use of Terminal Unipolar Electrogram Current of Injury as a Novel Marker to Estimate Contact: An Acute Canine Study.”
On July 10, 2017, the PURE EP System was featured in a poster presentation at the American Heart Association's 13th Annual Basic Cardiovascular Sciences (BCVS) 2017 Scientific Sessions: Pathways to Cardiovascular Therapeutics entitled, “Use of a Novel Electrogram Filtering Algorithm to Visualize Conduction Tissue Signals in the Ventricle in Sinus Rhythm and Arrhythmia: An Acute Canine Study.”
On July 11, 2017, the Company announced that it has engaged Health Research International (HRI) to compile essential market data and help perform strategic planning for its PURE EP™ platform technology.
On July 12, 2017, the PURE EP System was featured in a poster presentation at the American Heart Association’s 13th Annual Basic Cardiovascular Sciences (BCVS) 2017 Scientific Sessions: Pathways to Cardiovascular Therapeutics entitled, “Assessment of Catheter Position above or below the Aortic Valve by Evaluation of Characteristics of the Local Electro gram: An Acute Canine Study.”
On August 9, 2017, Dr. Asirvatham performed our tenth pre-clinical study at Mayo Clinic in Rochester, Minnesota.
On October 11, 2017, the Company announced that Mr. Joseph W. Rafferty has joined the Company as Chief Commercialization Officer.
On October 19, 2017, the Company announced that they have made significant progress towards commercialization of their proprietary PURE EP System and recently received the first production units of the PURE EP System from its manufacturing partner, Minnetronix.

On October 24, 2017, the Company announced that they have engaged Quintain Project Solutions LLC as the manufacturing project management leader for the PURE EP System.
On October 26, 2017, announced that the Company has concluded a key part of the strategic planning project launched earlier this year in collaboration with Health Research International (HRI). HRI conducted a detailed survey of U.S. electrophysiologists primarily based in New York, Texas, Massachusetts, Florida, Pennsylvania, and North Carolina. Among the factors interfering with effective ablations, the inability to record high quality unipolar signals and difficulty detecting small intracardiac signals were consistently reported. Survey respondents rated all six features listed of the PURE EP System as being ‘Very Helpful’ for their ablations, emphasizing overall noise reduction and improved signal clarity/accuracy as key benefits. Most respondents see signal clarity as paramount to the success of ablations and indicated interest in a technology that reduces ‘noise’.

We conducted our first, second and third pre-clinical studies on March 31, 2015, June 10, 2015, and November 17, 2015 respectively, and began additional pre-clinical studies as part of an advanced research program in June 2016, atevaluation with the PURE EP™ System under several protocols. At Mayo Clinic in Rochester, Minnesota, with the PURE EP System prototype. Wewe have performed twenty-seven experiments (including novel research programs such as Artificial Intelligence, or AI, and repolarization) in various animal models; we also conducted a pre-clinical study at the Mount Sinai Hospital in New York, NYNew York, with an emphasis on the ventricular tachycardia (VT) model.

We intendVT model; and six experiments to conductdate during a pre-clinical study at the Cardiac Arrhythmia Center at the University of California at Los Angeles with emphasis on the ventricular tachycardia (VT) model.Pennsylvania. We intend to conduct further pre-clinicalcontinue additional research and development studies end-user preference studies,with our technology at Mayo Clinic and research studies.other national centers.

In September 2021, we announced that we entered into a manufacturing and professional services agreement with Plexus Corp (“Plexus”) (Nasdaq: PLXS). Under the terms of the agreement, Plexus will manufacture the PURE EP™ System.

In December 2020, we announced that three PURE EP™ Systems were contracted for purchase by St. David’s Healthcare in Austin, Texas and were subsequently sold in February 2021. We also sold three PURE EP™ Systems to Mayo Foundation for Medical Education and Research in 2021 for use in Mayo Clinic campuses in Rochester, Minnesota, Jacksonville, Florida and Phoenix, Arizona.

On July 1, 2022, we entered into our first national purchasing agreement with HCA Management Services, L.P. whereby Kansas City Heart Institute at Overland Park Regional Medical Center in Kansas City, Missouri has acquired our technology under the terms of the new agreement with a 30-month lease of the system. The main objectiveagreement represents the first commercial adoption since we announced the national launch of these studiesour PURE EP™ System supported by our new commercial structure and clinical support teams.

In January 2022, we were awarded U.S. patent claims for our PURE EP™ noise-filtering technology which address computer-implemented systems and methods for filtering noise from input cardiac signals. We now have 49 worldwide patents owned or controlled by us covering our novel technology for arrhythmia care and electroporation.

ViralClear Pharmaceuticals, Inc.

ViralClear Pharmaceuticals, Inc. (“ViralClear”) is a majority-owned subsidiary of the Company originally known as NeuroClear Technologies, Inc. The subsidiary was established November 2018 to demonstrate the clinical potentialpursue additional applications of the PURE EP System.


EP™ signal processing technology outside of EP. In March 2020, it was renamed ViralClear to develop merimepodib, a broad-spectrum anti-viral agent that showed potential to treat COVID-19. We have initiated technology developmentcurrently do not intend to further develop merimepodib. Since late 2020, ViralClear has been realigned with Minnetronix, a medical technology and innovation company, and engaged Quintain Project Solutions LLC as the manufacturing project management leader forits original objective of pursuing additional applications of the PURE EP System - implementing steps for obtaining 510(k) clearance fromEP™ signal processing technology outside of cardiac electrophysiology. As of June 30, 2022, the U.S. Food and Drug Administration for the PURE EP System.Company retains 69.08% ownership of ViralClear.



We believe that by the first half of 2018, we will have obtained 510(k) marketing clearance from the FDA and will be able to commence marketing and commercialization of the PURE EP System. Our ability to achieve the aforementioned milestones will be principally determined by our ability to obtain necessary financing and regulatory approvals, among other factors.


We have chosen and are working with the National Standards Authority of Ireland (NSAI) as our Notified Body to obtain the CE Mark. CE marking is a mandatory approval for medical devices sold in Europe and Canada.  We plan on submitting for CE Mark in 2018.

Because we are a development stage company, with our initial product under development, we currently do not have any customers. We anticipate that our initial customers will be hospitals and other health care facilities that operate electrophysiology labs.

Results of Operations (000s)

We anticipate that our results of operations will fluctuate for the foreseeable future due to several factors, such as the progress of our research and development and commercialization efforts, and the timing and outcome of future regulatory submissions.submissions and uncertainty around the current pandemic. Due to these uncertainties, accurate predictions of future operations are difficult or impossible to make.


Three Months Ended SeptemberJune 30, 20172022 Compared to Three Months Ended SeptemberJune 30, 20162021 (000s)

Revenues and Cost of Goods Sold. We had no revenues or cost of goods sold duringRevenue for the three months ended SeptemberJune 30, 20172022 totaled $8 comprised of service revenue as compared to $207 for the three months ended June 30, 2021 comprised of product sales of $199 and 2016.recognized service revenue of $8.

We derive our revenue primarily from the sale of our medical device, PURE EP system, as well as related support and maintenance services and software upgrades in connection with the system.

We recognize revenue in accordance with Accounting Standards Codification (ASC) 606, Revenue from Contracts with Customers (“ASC 606”). The core principle of ASC 606 is that an entity recognizes revenue to depict the transfer of promised goods or services to customers in an amount that reflects the consideration to which the entity expects to be entitled in exchange for those goods or services.

Cost of goods sold for the three months ended June 30, 2022, was nil as compared to $62 for the three months ended June 30, 2021.

Gross profit from the three months ended June 30, 2022 was $8, or 100.0%, as compared to $145, or 70.0%, for the three months ended June 30, 2021.

In 2021, we had limited release of our product and our commercial launch is scheduled in latter part of 2022.

Research and Development Expenses. Research and development expenses for the three months ended SeptemberJune 30, 20172022 were $1,124,506, an increase$1,351, a decrease of $563,992,$316, or 100.6%19.0%, from $560,514$1,667 for the three months ended SeptemberJune 30, 2016. This increase2021. The decrease is primarily due additional personnel, outside design costs and current year acquiredto decreased research and developmentclinical studies, net with increased staffing levels for the three months ended June 30 2022 as we develop our proprietary technology platform.compared to three months ended June 30, 2021. Research and development expenses were comprised of the following:


Three months ended:


 
September 30,
2017
  
September 30,
2016
  

June 30, 2022

  

June 30, 2021

 
Salaries and equity compensation $272,014  $262,227  $1,108  $776 
Consulting expenses  123,271   85,510   40   165 
Clinical studies and design work  668,676   162,293 

Research and clinical studies and design work

  84   396 

Acquired Research and Development

  -   150 

Data/AI development

  28   84 

Regulatory

  9   9 
Travel, supplies, other  60,545   50,484   82   87 
Total $1,124,506  $560,514  $1,351  $1,667 

Stock based compensation for research and development personnel was $8,020$340 and $16,931$16 for the three months ended SeptemberJune 30, 20172022 and 2016,2021, respectively.


General and Administrative Expenses.General and administrative expenses for the three months ended SeptemberJune 30, 20172022 were $786,948,$4,302, a decrease of $204,904,$2,178, or 20.7%33.6%, from $991,852$6,480 incurred in the three months ended SeptemberJune 30, 2016.2021. This decrease is primarily due to a decreasereduction in stock based compensation issued to employeesthe activities of our ViralClear segment, net with an increase in employee performance pay and consultantsstaff in the current period as compared to the same period in the prior year and lessadditional service provider fees paid.

Payroll related expenses decreased to $260,125$2,042 in the current period from $292,275$2,124 for the three months ended SeptemberJune 30, 2016,2021, a decrease of $32,150.$82, or 3.9%. The decrease was primarily due to executive staff reductionchanges and mix in 2017.commercialization, sales and general and administration in the BioSig segment. We incurred $48,603$36 in stock basedstock-based compensation in connection with the vesting of stock and stock options issued to board members, officers, employees, and consultants for the three months ended SeptemberJune 30, 20172022, as compared to $223,986$1,965 in stock basedstock-based compensation for the same period in 2016.


2021, a decrease of $1,929 or 98.2%.

28


Professional services for the three months ended SeptemberJune 30, 20172022, totaled $53,708, an increase$166, a decrease of $4,532,$218, or 9.2%56.8%, overfrom the $49,176$384 recognized for the three months ended SeptemberJune 30, 2016.2021. Of professional services, legal fees totaled $34,458$130 for the three months ended SeptemberJune 30, 2017,2022, a decrease of $1,715,$118, or 4.7%47.6%, from $36,173$248 incurred for the three months ended SeptemberJune 30, 2016.2021. The decrease is primarily due to costs incurred in 2021 for financing, contract work and patent filings for the BioSig segment not incurred in current period. Accounting fees incurred in the three months ended SeptemberJune 30, 20172022, amounted to $19,250, an increase$36, a decrease of $6,250,$3, or 48.1%7.7%, from $13,000$39 incurred in same period lastthe prior year. The increase in legal fees was primarily due registration statements filed in 2017. In 2021, we incurred added audit costs for both the BioSig and ViralClear segments.


Consulting, public and investor relations fees for the three months ended SeptemberJune 30, 20172022 were $246,009$1,258 as compared to $226,065$758 incurred for the three months ended SeptemberJune 30, 2016.2021, an increase of $500, or 66.0%. The increase in consulting, marketing and investor relations fees during the three months ended SeptemberJune 30, 2017 relate2022 related to our continued efforts to develop our recognition throughout the medical industry in an effective manner.

Travel, meals and entertainment costs for the three months ended SeptemberJune 30, 20172022 were $85,222, an increase$265, a decrease of $36,622,$44, or 75.4%14.2%, from $48,600$309 incurred in the three months ended SeptemberJune 30, 2016.2021. Travel, meals and entertainment costs include travel related to business development and financing.

Rent for the three months ended SeptemberJune 30, 20172022 totaled $38,450, an increase$107, a decrease of $5,972$10, or 18.4%8.5%, from $32,478$117 incurred in three months ended June 30, 2021. The decrease in rent for 2022 as compared to 2021 is due primarily to a lower negotiated rent for our Los Angeles offices beginning July 1, 2021 and reduction of our rent in our Connecticut headquarters with our move to a larger facility in September 30, 2016. 2021 as compared to 2021.


Depreciation and Amortization Expense. Depreciation and amortization expense for the three months ended SeptemberJune 30, 20172022 totaled $2,834$71, an increase of $264,$22, or 10.3%44.9%, over the expense of $2,570$49 incurred in the three months ended SeptemberJune 30, 2016,2021, as a result of the replacement of aging ofadding additional office computers, manufacturing and other equipment.


Gain on change in fair values of derivatives.  Beginning in March 2015, we are required to estimate the fair value of the embedded beneficial conversion features of our issued Series C

Preferred Stock and certain warrants with reset (anti-dilution) provisions.  During the three months ended September 30, 2017, we incurred a gain on change in fair values of these derivatives of $113,724 as compared to a gain of $17,771 for the same period during the prior year.


Preferred Stock DividendDividends. Preferred stock dividend for the three months ended SeptemberJune 30, 20172022 and 2021 totaled $22,307,$3. Preferred stock dividends are related to the dividends accrued on our Series C Preferred Stock issued during the period from 2013 through 2015. In addition, the Series C Preferred stock conversion rate reset from $2.27 to $0.75 in 2022, therefore we recorded a decreasenoncash deemed preferred stock dividend of $2,419, or 9.8% from $24,726 incurred$108 during the three months ended SeptemberJune 30, 2016. Preferred stock dividends are primarily related to the issuance of our Series C Preferred Stock from 2013 through 2015.  The reduction in 2017 as compared to 2016 is the result of conversions of the Series C Preferred Stock.  2022.

Net Loss availableAttributable to common shareholdersBioSig Technologies, Inc. Common Shareholders. As a result of the foregoing, net loss availableattributable to common shareholders for the three months ended SeptemberJune 30, 20172022 was $1,822,856$5,870 compared to a net loss of $1,561,891$7,704 for the three months ended SeptemberJune 30, 2016.2021.


Nine

Six Months Ended SeptemberJune 30, 20172022 Compared to NineSix Months Ended SeptemberJune 30, 20162021 (000s)

Revenues and Cost of Goods Sold. Revenue for the six months ended June 30, 2022 totaled $16 comprised of service revenue as compared to $325 for the six months ended June 30, 2021 comprised of product sales of $314 and recognized service revenue of $11.

We had no revenuesderive our revenue primarily from the sale of our medical device, PURE EP system, as well as related support and maintenance services and software upgrades in connection with the system.

We recognize revenue in accordance with Accounting Standards Codification (ASC) 606, Revenue from Contracts with Customers (“ASC 606”). The core principle of ASC 606 is that an entity recognizes revenue to depict the transfer of promised goods or costservices to customers in an amount that reflects the consideration to which the entity expects to be entitled in exchange for those goods or services.

Cost of goods sold duringfor the ninesix months ended SeptemberJune 30, 20172022, was nil as compared to $161 for the six months ended June 30, 2021.

Gross profit from the six months ended June 30, 2022 was $16, or 100.0%, as compared to $164, or 50.5%, for the six months ended June 30, 2021.

In 2021, we had limited release of our product and 2016.our commercial launch is scheduled in latter part of 2022.

Research and Development Expenses. Research and development expenses for the ninesix months ended SeptemberJune 30, 20172022 were $3,802,149,$2,968, an increase of $1,662,478,$35, or 77.7%1.2%, from $2,139,671$2,933 for the ninesix months ended SeptemberJune 30, 2016. This increase is primarily due additional personnel, outside design costs and current year acquired research and development as we develop our proprietary technology platform.2021. Research and development expenses were comprised of the following:


Nine

Six months ended:


  
September 30,
2017
  
September 30,
2016
 
Salaries and equity compensation $824,056  $1,491,448 
Consulting expenses  371,956   249,874 
Clinical studies and design work  1,910,271   221,305 
Acquired research and development  543,927   - 
Travel, supplies, other  151,939   177,044 
  Total $3,802,149  $2,139,671 

29
  

June 30, 2022

  

June 30, 2021

 

Salaries and equity compensation

 $2,159  $1,275 

Consulting expenses

  171   354 

Research and clinical studies and design work

  196   691 

Acquired Research and Development

  -   150 

Data/AI development

  78   211 

Regulatory

  29   68 

Product development

  -   15 

Travel, supplies, other

  335   169 

Total

 $2,968  $2,933 


Stock based compensation for research and development personnel was $29,144$713 and $752,713$83 for the ninesix months ended SeptemberJune 30, 20172022 and 2016,2021, respectively.


On March 15, 2017, we entered into a know-how license agreement with Mayo Foundation for Medical Education and Research whereby we were granted an exclusive license, with the right to sublicense, certain know how and patent applications in the field of signal processing, physiologic recording, electrophysiology recording, electrophysiology software and autonomics to develop, make and offer for sale.  The agreement expires in ten years from the effective date.  As such, we are obligated to pay to Mayo Foundation a 1% or 2% royalty payment on net sales of licensed products, as defined.

In consideration, we issued 630,000 warrants to acquire the Company’s common stock at an exercise price of $1.50, expiring on March 15, 2020.  The estimated fair value of $543,927 was charged to operations as acquired research and development.

General and Administrative Expenses.General and administrative expenses for the ninesix months ended SeptemberJune 30, 20172022 were $4,020,625,$10,703, a decrease of $3,237,227,$3,048, or 44.6%22.2%, from $7,257,852$13,751 incurred in the ninesix months ended SeptemberJune 30, 2016.2021. This decrease is primarily due to a decreasereduction in stock based compensation issued to employeesthe activities of our ViralClear segment, net with an increase in employee performance pay and consultantsstaff in the current period as compared to the same period in the prior year and lessadditional service provider fees paid.


Payroll related expenses increased to $1,004,717$4,574 in the current period from $894,995$3,973 for the ninesix months ended SeptemberJune 30, 2016,2021, an increase of $109,722.$601, or 15.1%. The increase was primarily due to added personnelstaff in commercialization, sales and bonuses paidgeneral and administration in 2017.the BioSig segment. We incurred $1,110,338$1,469 in stock basedstock-based compensation in connection with the vesting of stock and stock options issued to board members, officers, employees and consultants for the ninesix months ended SeptemberJune 30, 20172022 as compared to $4,717,458$4,551 in stock basedstock-based compensation for the same period in 2016.2021.


Professional services for the ninesix months ended SeptemberJune 30, 20172022, totaled $284,058, an increase$506, a decrease of $23,068,$258, or 8.8%33.8%, overfrom the $260,990$764 recognized for the ninesix months ended SeptemberJune 30, 2016.2021. Of professional services, legal fees totaled $210,058$363 for the ninesix months ended SeptemberJune 30, 2017, an increase2022; a decrease of $16,568,$193, or 8.6%34.7%, from $193,490$556 incurred for the ninesix months ended SeptemberJune 30, 2016.2021. The decrease is primarily due to costs incurred in 2021 for financing, contract work and patent filings for the BioSig segment not incurred in current period. Accounting fees incurred in the ninesix months ended SeptemberJune 30, 20172022, amounted to $74,000,$143, an increase of $6,500,$32, or 9.6%28.8%, from $67,500$111 incurred in same period lastthe prior year. The increase in legal fees was primarily due to filing of registration statements in 2017 relating to our equity private placementsIn 2022, we incurred added audit costs for both the BioSig and assistance with our know how agreements entered into in 2017. ViralClear segments.


Consulting, public and investor relations fees for the ninesix months ended SeptemberJune 30, 20172022 were $1,103,819$1,380 as compared to $971,932$2,132 incurred for the ninesix months ended SeptemberJune 30, 2016.2021, a decrease of $752, or 35.3%. The increasedecrease in consulting, marketing and investor relations fees during the ninesix months ended SeptemberJune 30, 2017 relate2022 related to our continuedefficient efforts to develop our recognition throughout the medical industry.industry in an effective manner.

Travel, meals and entertainment costs for the ninesix months ended SeptemberJune 30, 20172022 were $250,122,$564, an increase of $54,244,$146, or 27.7%34.9%, from $195,878$418 incurred in the ninesix months ended SeptemberJune 30, 2016.2021. Travel, meals and entertainment costs include travel related to business development and financing. The increase in 2022 was due to the lifting of various restrictions imposed by the COVID-19 outbreak leading to increased commercialization effort in 2022 as compared to 2021.

Rent for the ninesix months ended June 30, 2022 totaled $213, a decrease of $21, or 9.0%, from $234 incurred in six months ended June 30, 2021. The decrease in rent for 2022 as compared to 2021 is due primarily to a lower negotiated rent for our Los Angeles offices beginning July 1, 2021 and reduction of our rent in our Connecticut headquarters with our move to a larger facility in September 2021 as compared to 2021.

Depreciation and Amortization Expense. Depreciation and amortization expense for the six months ended June 30, 20172022 totaled $101,859,$126, an increase of $5,346$35, or 5.5%, from $96,513 incurred in nine months ended September 30, 2016. 


Depreciation Expense. Depreciation expense for the nine months ended September 30, 2017 totaled $8,900, an increase of $1,089, or 13.9%38.5%, over the expense of $7,811$91 incurred in the ninesix months ended SeptemberJune 30, 2016,2021, as a result of the replacement of aging ofadding additional office computers, manufacturing and other equipment.


Loss on change in fair values of derivatives.  Beginning in March 2015, we are required to estimate the fair value of the embedded beneficial conversion features of our issued Series C Preferred Stock and certain warrants with reset (anti-dilution) provisions.  During the nine months ended September 30, 2017, we incurred a loss on change in fair values of these derivatives of $320,131 as compared to a loss of $807,087 for the same period during the prior year.

Preferred Stock Dividend. Preferred stock dividend for the ninesix months ended SeptemberJune 30, 20172022 and 2021 totaled $68,915, a decrease of $16,552, or 19.4% from $85,467 incurred during the nine months ended September 30, 2016.$5. Preferred stock dividends are primarily related to the issuance ofdividends accrued on our Series C Preferred Stock issued during the period from 2013 through 2015. The reduction in 2017 as compared to 2016 is the result of conversions ofIn addition, the Series C Preferred Stock.  

stock conversion rate reset from $2.27 to $0.75 in 2022, therefore we recorded a noncash deemed preferred stock dividend of $108 during the six months ended June 30, 2022.

30


Net Loss availableAttributable to common shareholdersBioSig Technologies, Inc. Common Shareholders. As a result of the foregoing, net loss availableattributable to common shareholders for the ninesix months ended SeptemberJune 30, 20172022 was $8,220,651$13,835 compared to a net loss of $10,297,887$16,025 for the ninesix months ended SeptemberJune 30, 2016.2021.

Segment Results

The Company reports segment information based on the “management” approach. The management approach designates the internal reporting used by management for making decisions and assessing performance as the source of the Company’s reportable segments.

Summary Statement of Operations for the three and six months ended June 30, 2022 as compared to the three and six months ended June 30, 2021 are detailed in Note 11 of the accompanying unaudited condensed consolidated financial statements.

COVID-19

On March 11, 2020, the World Health Organization (the “WHO”) declared a pandemic related to the rapidly spreading coronavirus (COVID-19) outbreak, which has led to a global health emergency. The full public-health impact of the ongoing pandemic is currently indeterminable and rapidly evolving, and the related health crisis has adversely affected and may continue to adversely affect the global economy, resulting in delays to our commercialization objectives of the PURE EP Systems into mid-2022.

Liquidity and Capital Resources ($000s)

Nine Months Ended September 30, 2017 Compared to nine Months Ended September 30, 2016

As of SeptemberJune 30, 2017,2022, we had a working capital deficit (current liabilities in excess of current assets) of $3,839,317,$5,837, comprised of cash of $234,285$5,077, inventory of $2,026 and prepaid expenses and vendor deposits of $150,482,$633, which was offset by $1,301,603$1,451 of accounts payable and accrued expenses, accrued dividends on preferred stock issuances of $396,939$86 and an aggregatecurrent portions of $2,525,542deferred revenue of warrant$21 and derivative liabilities. Excluding the warrant and derivative liabilities, the Company’s working capital deficit would have been $1,313,775.of lease liability of $341. For the ninesix months ended SeptemberJune 30, 2017,2022, we used $5,215,666$12,644 of cash in operating activities and $6,788$60 of cash in investing activities.


Six Months Ended June 30, 2022 Compared to Six Months Ended June 30, 2021 (000s)

Cash provided by financing activities totaled $4,400,844,$6,122, comprised of proceeds from the sale of our common stock and receiptwarrants under direct offerings of $5,820, net of expenses of $441, and $302 from the sale of our common stock subscriptions. under our at-the-market offering, net of expenses of $46.

In the comparable period in 2016,2021, our aggregate cash provided by financing activities totaled $3,053,868$1,328, comprised of proceeds from the sale of our common stock.stock in an at-the-market offering of $1,300 and proceeds from exercise of options of $28. At SeptemberJune 30, 2017,2022, we had cash of $234,285$5,077 compared to $1,055,895$15,504 at December 31, 2016.June 30, 2021. Our cash is held in bank deposit accounts. At SeptemberJune 30, 20172022 and December 31, 2016,June 30, 2021, we had no convertible debentures outstanding.


Cash used in operations for the ninesix months ended SeptemberJune 30, 20172022 and 20162021 was $5,215,666$12,644 and $3,844,553,$13,910, respectively, which represent cash outlays for research and development and general and administrative expenses in such periods. The increasedecreases in cash outlays principally resulted from additional inreduced operating costs, and general and administrative expenses netin 2022 and with an increaseincreases in our operating assets of $422 and decreases in our outstanding accounts payable by $930,110.operating liabilities of $914.


We used $6,788$60 cash for investing activities for the ninesix months ended SeptemberJune 30, 2017,2022, compared to $12,095$182 for the ninesix months ended SeptemberJune 30, 2016.2021. For both periods,the current period and comparable period, we purchased computer and other equipment.


In their report dated March

We had an accumulated deficit as of June 30, 2017,2022, of $202, 750, as well as a net loss attributable to BioSig Technologies, Inc. of $13,833 and negative operating cash flows. We expect to continue incurring losses and negative cash flows from operations until our independent registered public accounting firm stated at December 31, 2016, there isproducts (primarily our PURE EP System) reach full commercial profitability.

These conditions raise substantial doubt about our ability to continue as a going concern. Our ability to continue as a going concern is an issue raised due to our net losses and negative cash flows from operations since inception and our expectation is that these conditions will continue for the foreseeable future. In addition, weWe will require additional financing to fund future operations.


Further, Although we do not have any commercial products available for sale, andwe have not generated significant revenues to date, and there is no assurance that if approval of our products is received, we will be able to generate cash flow to fund operations. In addition, there can be no assurance that our research and development will be successfully completed or that any productadditional products will be approved or commercially viable. Our ability to continue as a going concern is subject to our ability to obtain necessary funding from outside sources, including obtaining additional funding from the sale of our securities, obtaining loans from various financial institutions or being awarded grants from government agencies, where possible. Our continued net operating losses increase the difficulty in meeting such goals and there can be no assurances that such methods will prove successful.

Our plans include the continued commercialization of the PURE EP System and other applications of our core technology and raising capital through the sale of additional equity securities, debt or capital inflows from strategic partnerships. Our shift from a focus on technology development to commercialization has allowed us to reduce our annual expenses in a meaningful way. As a result of this transition, we have been able to achieve savings through reductions in executive and management compensation and a reduction of our utilization of external consultants and professional service providers. We believe these cost-saving measures combined with our expectations of positive trends in commercial activity create the potential for us to achieve a lower cash flow breakeven rate. There are no assurances, however, that we will be successful in obtaining the level of financing needed for our operations.

The ongoing COVID-19 pandemic has resulted and continues to result in significant financial market volatility and uncertainty in recent months. In addition, U.S. and global markets are experiencing volatility and disruption following the escalation of geopolitical tensions and the ongoing military conflict between Russia and Ukraine.

A continuation or worsening of the levels of market disruption and volatility seen in the recent past could have an adverse effect on our ability to access capital and on the market price of our common stock, and we may not be able to successfully raise capital through the sale of our securities.

Our Series C Preferred Stock contains triggering events which would, among other things, require redemption (i) in cash, at the greater of (a) 120% of the stated value of $1 or (b) the product of (I) the variable weighted average price of our common stock on the trading day immediately preceding the date of the triggering event and (II) the stated value divided by the then conversion price or (ii) in shares of our common stock, equal to a number of shares equal to the amount set forth in (i) above divided by 75%. As of June 30, 2022, the aggregate stated value of our Series C Preferred Stock was $105. The triggering events include our being subject to a judgment of greater than $100 or our initiation of bankruptcy proceedings. If any of the triggering events contained in our Series C Preferred Stock occur, the holders of our Series C Preferred Stock may demand redemption, an obligation we may not have the ability to meet at the time of such demand. We will be required to pay interest on any amounts remaining unpaid after the required redemption of our Series C Preferred Stock, at a rate equal to the lesser of 18% per annum or the maximum rate permitted by applicable law.

We expect to incur losses from operations for the near future. We expect to incur increasing marketing and commercialization expenses related to our PURE EP system in addition to additional research and development expenses,costs relating to the PURE EP and other product candidates, including expenses related to clinical trials. We expect that our general and administrative expenses will increase in the future as we expand our business development, add infrastructure and incur additional costs related to being a public company, including incremental audit fees, investor relations programs and increased professional services.


Our future capital requirements will depend on a number of factors, including the progress of our research and development of product candidates, the timing and outcome of regulatory approvals, the costs involved in preparing, filing, prosecuting, maintaining, defending and enforcing patent claims and other intellectual property rights, the status of competitive products, the availability of financing and our success in developing markets for our product candidates. We believe our existing cash will not be sufficient to fund our operating expenses and capital equipment requirements. We anticipate we will need approximately $4 million in addition to our current cash on hand to fund our operating expenses and capital equipment requirements for the next 12 months.



We will have to raise additional funds to continue our operations and, while we have been successful in doing so in the past, there can be no assurance that we will be able to do so in the future. Our continuation as a going concern is dependent upon our ability to obtain necessary additional funds to continue operations and the attainment of profitable operations.

Future financing may include the issuance of equity or debt securities, obtaining credit facilities, or other financing mechanisms. Even if we are able to raise the funds required, it is possible that we could incur unexpected costs and expenses or experience unexpected cash requirements that would force us to seek alternative financing. Furthermore, if we issue additional equity or debt securities, existing holders of our securities may experience additional dilution or the new equity securities may have rights, preferences or privileges senior to those of existing holders of our securities.

If additional financing is not available or is not available on acceptable terms, we may be required to delay, reduce the scope of or eliminate our research and development programs, reduce our commercialization efforts or obtain funds through arrangements with collaborative partners or others that may require us to relinquish rights to certain product candidates that we might otherwise seek to develop or commercialize independently.


Equity Financing

Off-Balance Sheet Arrangements

ATM Sales Agreement

We do not have any off-balance sheet arrangements.

Transactions

On May 17, 2022, the Company entered into an ATM Sales Agreement (the “Sales Agreement”) with Related Parties


TheVirtu Americas LLC to act as the Company’s President and shareholders have advanced fundssales agent or principal (“Agent”), with respect to the Company for working capital purposes sinceissuance and sale of up to $10.0 million of the Company’s inceptionshares of common stock, par value $0.001 per share (the “Shares”), from time to time in February 2009.  No formal repaymentan at-the-market public offering.

Upon delivery of a placement notice and subject to the terms and conditions of the Sales Agreement, Virtu Americas LLC may sell the common stock by any method permitted by law deemed to be an “at the market offering” as defined in Rule 415(a)(4) promulgated under the Securities Act of 1933, as amended (the “Securities Act”). The Company may sell the common stock in amounts and at times to be determined by the Company from time to time subject to the terms and conditions of the Sales Agreement, but it has no obligation to sell any of the common stock under the Sales Agreement. The Company or arrangements existVirtu Americas LLC may suspend or terminate the offering of common stock upon notice to the other party and subject to other conditions. Virtu Americas LLC will act as sales agent on a commercially reasonable efforts basis consistent with its normal trading and sales practices and applicable state and federal law, rules and regulations and the rules of Nasdaq.

The Company is not accruing interestwill pay Agent a commission of up to 3.0% of the gross proceeds from the sale of the common stock pursuant to the Sales Agreement.

The offering of common stock pursuant to the Sales Agreement will terminate upon the earlier of (i) the sale of all common stock subject to the Sales Agreement or (ii) termination of the Sales Agreement in accordance with its terms.

The common stock was sold and issued pursuant the Company’s shelf registration statement on these advances. The net amountForm S-3 (File No. 333-251859), which was previously declared effective by the Securities and Exchange Commission, and a related prospectus.

Sale of outstanding advances at September 30, 2017 and December 31, 2016 was $-0-.common stock


At September 30, 2017 and December 31, 2016,

On June 24, 2022, the Company had reimbursable travelentered into an underwriting agreement (the “Underwriting Agreement”) with Laidlaw & Company (UK) Ltd. (the “Underwriter”), which was amended and restated on June 28, 2022 (the “Amended and Restated Underwriting Agreement”), relating to a best-efforts public offering of 4,341,667 shares of the Company’s common stock (the “Shares”). The public offering price of the Shares was $0.75 per share. After the underwriting discounts, which includes a reduced discount with respect to certain Company-introduced investors, and offering expenses, the Company received net proceeds from the offering of approximately $2,818,000.

Pursuant to the Amended and Restated Underwriting Agreement, the Company issued to the Underwriter, or its designees warrants to purchase up to an aggregate 217,083 shares of common stock, or 5% of the number of common stock sold in the offering. The underwriter warrants are exercisable following the date of issuance and ending five years from the date of the execution of the Underwriting Agreement, at a price per share equal to $0.90 per share (120% of the public offering price per share) and are exercisable on a “cashless” basis. The Company also agreed to reimburse the Underwriter for certain of their out-of-pocket expenses incurred in connection with the offering, including, among other relatedthings, the reasonable fees and expenses due related parties of $17,888counsel, which fees and $15,755, respectively.expenses may not exceed $125,000.


The Shares were sold and issued pursuant to the Company’s shelf registration statement on Form S-3 (Registration Statement No. 333-251859) previously filed with the Securities and Exchange Commission and declared effective by the Securities and Exchange Commission on January 12, 2021. A preliminary prospectus supplement and prospectus supplement and the accompanying prospectus relating to the offering have been filed with the Securities and Exchange Commission. The offering closed on June 29, 2022.

Critical Accounting Policies and Estimates

Our discussion and analysis of our financial condition and results of operations are based on our financial statements, which have been prepared in accordance with accounting principles generally accepted in the United States of America. The preparation of these financial statements requires us to make estimates and judgments that affect the reported amounts of assets, liabilities and expenses. We evaluate our estimates and judgments on an ongoing basis. We base our estimates on historical experience and on assumptions that we believe to be reasonable under the circumstances, the results of which form the basis for making judgments about the carrying values of assets and liabilities that are not readily apparent from other sources. Actual results may differ from these estimates.


We believe the following critical accounting policies affect our more significant judgments and estimates used in the preparation of our financial statements.

Revenue Recognition

We derive our revenue primarily from the sale of our medical device, the PURE EP™ System, as well as related support and maintenance services and software upgrades in connection with the system.

We recognize revenue in accordance with Accounting Standards Codification (ASC) 606, Revenue from Contracts with Customers (“ASC 606”). The core principle of ASC 606 is that an entity recognizes revenue to depict the transfer of promised goods or services to customers in an amount that reflects the consideration to which the entity expects to be entitled in exchange for those goods or services.

We determine revenue recognition through the following five steps:

Identify the contract with the customer;

Identify the performance obligations in the contract;

Determine the transaction price;

Allocate the transaction price to the performance obligation in the contract; and

Recognize revenue when, or as, the performance obligations are satisfied.

Performance obligations are the unit of accounting for revenue recognition and generally represent the distinct goods or services that are promised to the customer. If we determine that it has not satisfied a performance obligation, it will defer recognition of the revenue until the performance obligation is deemed to be satisfied. Support, maintenance, and software upgrades are performance obligations over a defined period and are recognized ratably over the contractual service period. Customers typically purchase these services with the initial sale of the PURE EP System and do not have the right to terminate their contracts unless we fail to perform material obligations.

We may execute more than one contract with a single customer. If so, it is evaluated whether the agreements were negotiated as a package with a single objective, whether the amount of consideration to be paid in one agreement depends on the price and/or performance of another agreement, or whether the goods or services promised in the agreements represent a single performance obligation. The conclusions reached can impact the allocation of the transaction price to each performance obligation and the timing of revenue recognition related to those arrangements.

We estimate the transaction price based on the amount of consideration we expect to receive for transferring the promised goods or services in the contract. The consideration may include both fixed consideration and variable consideration. At the inception of each arrangement that includes variable consideration, we evaluate the amount of the potential payments and the likelihood that the payments will be received. If it is probable that a significant revenue reversal would not occur, the variable consideration is included in the transaction price.

We record accounts receivable for amounts invoiced to customers for which the Company has an unconditional right to consideration as provided under the contractual arrangement. Unbilled receivables, if any, include amounts related to our contractual right to consideration for completed performance obligations not yet invoiced. Deferred revenue includes payments received in advance of performance under the contract. Our unbilled receivables and deferred revenue are reported on an individual contract basis at the end of each reporting period. Unbilled receivables are classified as current or noncurrent based on the timing of when we expect to bill the customer. Deferred revenue is classified as current or noncurrent based on the timing of when we expect to recognize revenue.

Research and Development.

We account for research and development costs in accordance with the Accounting Standards Codification subtopic 730-10, Research and Development (“ASC 730-10”). Under ASC 730-10, all research and development costs must be charged to expense as incurred. Accordingly, internal research and development costs are expensed as incurred. Third-party research and developmentsdevelopment costs are expensed when the contracted work has been performed or as milestone results have been achieved. Company-sponsored research and development costs related to both present and future products are expensed in the period incurred.



Stock Based Compensation.

All stock-based payments to employees and to nonemployee directors for their services as directors consisted of grants of restricted stock and stock options, which are measured at fair value on the grant date and recognized in the statements of operations as compensation expense over the relevant vesting period. Restricted stock payments and stock-based payments to nonemployees are recognized as an expense over the period of performance.

Such payments are measured at fair value at the earlier of the date a performance commitment is reached, or the date performance is completed. In addition, for awards that vest immediately and are non-forfeitable, the measurement date is the date the award is issued.

On October 29, 2014, our common stock commenced trading on OTCQB under the symbol “BSGM.”  Fair value is typically determined by the closing price of our common stock on the date of the award.
Income Taxes.
Deferred income tax assets and liabilities are determined based on the estimated future tax effects of net operating loss and credit carryforwards and temporary differences between the tax basis of assets and liabilities and their respective financial reporting amounts measured at the current enacted tax rates. We record an estimated valuation allowance on our deferred income tax assets if it is not more likely than not that these deferred income tax assets will be realized. We recognize a tax benefit from an uncertain tax position only if it is more likely than not that the tax position will be sustained on examination by taxing authorities, based on the technical merits of the position. The tax benefits recognized in the financial statements from such a position are measured based on the largest benefit that has a greater than 50% likelihood of being realized upon ultimate settlement.

Derivative and Warrant Liabilities.

We account for derivative instruments in accordance with ASC 815, which establishes accounting and reporting standards for derivative instruments and hedging activities, including certain derivative instruments embedded in other financial instruments or contracts and requires recognition of all derivatives on the balance sheet at fair value, regardless of hedging relationship designation. Accounting for changes in fair value of the derivative instruments depends on whether the derivatives qualify as hedge relationships and the types of relationships designated are based on the exposures hedged. At September 30, 2017 and December 31, 2016, we did not have any derivative instruments that were designated as hedges.

ITEM 3. QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK

Not required under Regulation S-K for “smaller reporting companies.”


ITEM 4. CONTROLS AND PROCEDURES


Evaluation of Disclosure Controls and Procedures

As required under Rules 13a-15(e) and 15d-15(e) under the Securities Exchange Act of 1934, as amended (the “Exchange Act”), we carried out an evaluation, under the supervision and with the participation of our management, including our Chief Executive Officer and Chief Financial Officer, of the effectiveness of the design and operation of our disclosure controls and procedures (as defined under Rule 13a-15(e) under the Exchange Act) as of September 30, 2017.the end of the period covered by this report. Based upon that evaluation, theour Chief Executive Officer and Chief Financial Officer concluded that our disclosure controls and procedures were effective to ensure that information required to be disclosed by us in the reports that we file or submit under the Exchange Act, is recorded, processed, summarized and reported, within the time periods specified in the Securities and Exchange Commission’s rules and forms, and that such information is accumulated and communicated to our management, including our Chief Executive Officer and Chief Financial Officer, as of September 30, 2017 were not effective, for the same reasons as previously disclosed under Item 9A. “Controls and Procedures” in our Annual Report on Form 10-K for our fiscal year ended December 31, 2016. appropriate, to allow timely decisions regarding required disclosure.


Changes in Internal Controls over Financial Reporting

There have been no changes in our internal controls over financial reporting (as defined in Rule 13a-15(f) and 15d-(f) of the Exchange Act) that occurred during the our last fiscal quarter to which this report relates that have materially affected, or are reasonably likely to materially affect, our internal control over financial reporting.




PART II –II. OTHER INFORMATION


ITEM 1. LEGAL PROCEEDINGS

From time to time, we may become involved in various lawsuits and legal proceedings which arise in the ordinary course of business. However, litigation is subject to inherent uncertainties, and an adverse result in such matters may arise from time to time that may harm our business. We are currently not aware of any such legal proceedings or claims that we believe will have, individually or in the aggregate, a material adverse effect on our business, financial condition or operating results.

There are no material proceedings in which any of our directors, officers or affiliates or any registered or beneficial shareholder of more than 5% of our common stock is an adverse party or has a material interest adverse to our interest.

None.

ITEM 1A. RISK FACTORS

The following description of risk factors includes any material changes to risk factors associated with our business, financial condition and results of operations previously disclosed in Item 1A. “Risk Factors” of our annual report on Form 10-K for the fiscal year ended December 31, 2021, as filed with the SEC on March 31, 2022. Our business, financial condition and operating results can be affected by a number of factors, whether currently known or unknown, including but not limited to those described below, any one or more of which could, directly or indirectly, cause our actual financial condition and operating results to vary materially from past, or from anticipated future, financial condition and operating results. Any of these factors, in whole or in part, could materially and adversely affect our business, financial condition, operating results, and stock price.

The following discussion of risk factors contains forward-looking statements. These risk factors may be important to understanding other statements in this Form 10-Q. The following information should be read in conjunction with the condensed consolidated financial statements and related notes in Part I, Item 1, “Financial Statements” and Part I, Item 2, “Management’s Discussion and Analysis of Financial Condition and Results of Operations” of this Form 10-Q.

The COVID-19 pandemic and related U.S. supply chain issues, including shipping and raw material disruptions, could have a continuing material impact on the global supply chain, which could adversely impact our business results and financial condition.

We rely on a limited number of suppliers and manufacturers, particularly in the production and service of our PURE EP™ System. In the event of interruption within our supply chain due to global shortages of key supplies, materials or products, we may not be able to increase capacity from other sources or develop alternative or secondary sources without incurring substantial additional costs and/or delays.

Prolonged shortages in raw material supplies, delays and disruptions to manufacturing, production and shipping, congestion at key shipping ports and shortages in warehouse storage space due to the supply chain crisis, could significantly and adversely affect our business if one or more of our manufacturers or suppliers are impacted by any interruption at a particular location or in relation to a particular material or component. To the extent the disruptions in the U.S. supply chain continue, our business, particularly the manufacturing of the PURE EP™ System, could be adversely affected.

Not

Our failure to meet the continued listing requirements of Nasdaq could result in a delisting of our common stock, which could negatively impact the market price and liquidity of our common stock and our ability to access the capital markets.

Our common stock is listed on the Nasdaq Capital Market. If we fail to satisfy the continued listing requirements of Nasdaq, such as minimum bid price requirements, Nasdaq may take steps to delist our common stock. Such a delisting would have a negative effect on the price of our common stock, impair the ability to sell or purchase our common stock when persons wish to do so, and any delisting materially adversely affect our ability to raise capital or pursue strategic restructuring, refinancing or other transactions on acceptable terms, or at all. Delisting from the Nasdaq Capital Market could also have other negative results, including the potential loss of institutional investor interest and fewer business development opportunities. In the event of a delisting, we would attempt to take actions to restore our compliance with Nasdaq’s listing requirements, but we can provide no assurance that any such action taken by us would allow our common stock to become listed again, stabilize the market price or improve the liquidity of our common stock, prevent our common stock from dropping below the Nasdaq minimum bid price requirement or prevent future non-compliance with Nasdaq’s listing requirements.

On July 14, 2022, we received a letter from the Listing Qualifications Department of Nasdaq indicating that, based upon the closing bid price of our common stock for the 30 consecutive business day period between May 31, 2022, through July 13, 2022, we did not meet the minimum bid price of $1.00 per share required under Regulation S-K for “smaller reporting companies.”continued listing on The Nasdaq Capital Market pursuant to Nasdaq Listing Rule 5550(a)(2). The letter also indicated that we will be provided with a compliance period of 180 calendar days, or until January 10, 2023 (the “Compliance Period”), in which to regain compliance pursuant to Nasdaq Listing Rule 5810(c)(3)(A).

In order to regain compliance with Nasdaq’s minimum bid price requirement, our common stock must maintain a minimum closing bid price of $1.00 for at least ten consecutive business days during the Compliance Period. In the event we do not regain compliance by the end of the Compliance Period, we may be eligible for additional time to regain compliance. To qualify, we will be required to meet the continued listing requirement for the market value of its publicly held shares and all other initial listing standards for The Nasdaq Capital Market, with the exception of the bid price requirement, and will need to provide written notice of its intention to cure the deficiency during the second compliance period, by effecting a reverse stock split if necessary. If we meet these requirements, we may be granted an additional 180 calendar days to regain compliance. However, if it appears to Nasdaq that we will be unable to cure the deficiency, or if we are not otherwise eligible for the additional cure period, Nasdaq will provide notice that our common stock will be subject to delisting.


ITEM 2. UNREGISTERED SALES OF EQUITY SECURITIES AND USE OF PROCEEDS

None.

On July 13, 2017, we consummated one closing under the Unit Purchase Agreement, dated April 6, 2017, by and among certain accredited investors (as defined by Rule 501 under the Securities Act of 1933, as amended), pursuant to which we issued 267,002 shares of our common stock and 133,501 warrants to purchase one share of our common stock, exercisable at a price of $1.50 per share and expiring July 13, 2020, in exchange for aggregate consideration of $400,380, net of $123 in expenses. The securities sold in this offering were not registered under the Securities Act of 1933, as amended, or the securities laws of any state, and were offered and sold in reliance on the exemption from registration under the Securities Act of 1933, as amended, provided by Section 4(2) and Regulation D (Rule 506) under the Securities Act of 1933, as amended.

On August 18, 2017, we consummated one closing under the Unit Purchase Agreement, dated April 6, 2017, by and among certain accredited investors (as defined by Rule 501 under the Securities Act of 1933, as amended), pursuant to which we issued 351,000 shares of our common stock and 175,500 warrants to purchase one share of our common stock, exercisable at a price of $1.50 per share and expiring August 18, 2020, in exchange for aggregate consideration of $526,212, net of $288 in expenses. The securities sold in this offering were not registered under the Securities Act of 1933, as amended, or the securities laws of any state, and were offered and sold in reliance on the exemption from registration under the Securities Act of 1933, as amended, provided by Section 4(2) and Regulation D (Rule 506) under the Securities Act of 1933, as amended.

On September 18, 2017, we consummated one closing under the Unit Purchase Agreement, dated April 6, 2017, by and among certain accredited investors (as defined by Rule 501 under the Securities Act of 1933, as amended), pursuant to which we issued 103,334 shares of our common stock and 51,668 warrants to purchase one share of our common stock, exercisable at a price of $1.50 per share and expiring September 18, 2020, in exchange for aggregate consideration of $154,940, net of $61 in expenses. The securities sold in this offering were not registered under the Securities Act of 1933, as amended, or the securities laws of any state, and were offered and sold in reliance on the exemption from registration under the Securities Act of 1933, as amended, provided by Section 4(2) and Regulation D (Rule 506) under the Securities Act of 1933, as amended.

ITEM 3. DEFAULTS UPON SENIOR SECURITIES

None.

None.

ITEM 4. MINE SAFETY DISCLOSURES

None.

None.

ITEM 5. OTHER INFORMATION

None.

None.


ITEM 6. EXHIBITS


31.01

Exhibit No.

Description

1.1

ATM Sales Agreement, dated May 17, 2022, by and between BioSig Technologies, Inc. and Virtu Americas LLC (incorporated by reference to Exhibit 1.1 to the Form 8-K filed on May 17, 2022)

1.2

Underwriting Agreement, dated June 24, 2022, by and between BioSig Technologies, Inc. and Laidlaw & Company (UK) Ltd. (incorporated by reference to Exhibit 1.1 to the Form 8-K filed on June 29, 2022)

1.3

Amended and Restated Underwriting Agreement, dated June 28, 2022, by and between BioSig Technologies, Inc. and Laidlaw & Company (UK) Ltd. (incorporated by reference to Exhibit 1.2 to the Form 8-K filed on June 29, 2022)

3.1

Amended and Restated Certificate of Incorporation of BioSig Technologies, Inc. (incorporated by reference to Exhibit 3.1 to the Form S-1 filed on July 22, 2013)

3.2

Certificate of Amendment to the Amended and Restated Certificate of Incorporation of BioSig Technologies, Inc. (incorporated by reference to Exhibit 3.2 to the Form S-1 filed on July 22, 2013)

3.3

Certificate of Second Amendment to the Amended and Restated Certificate of Incorporation of BioSig Technologies, Inc. (incorporated by reference to Exhibit 3.3 to the Form S-1 filed on July 22, 2013)

3.4

Certificate of Third Amendment to the Amended and Restated Certificate of Incorporation of BioSig Technologies, Inc. (incorporated by reference to Exhibit 3.5 to the Form S-1/A filed on January 21, 2014)

3.5

Certificate of Fourth Amendment to the Amended and Restated Certificate of Incorporation of BioSig Technologies, Inc. (incorporated by reference to Exhibit 3.6 to the Form S-1/A filed on March 28, 2014)

3.6

Certificate of Fifth Amendment to the Amended and Restated Certificate of Incorporation of BioSig Technologies, Inc. (incorporated by reference to Exhibit 3.1 to the Form 8-K filed on August 21, 2014)

3.7

Certificate of Sixth Amendment to the Amended and Restated Certificate of Incorporation of BioSig Technologies, Inc. (incorporated by reference to Exhibit 3.1 to the Form 8-K filed on November 25, 2016)

3.8

Certificate of Seventh Amendment to the Amended and Restated Certificate of BioSig Technologies, Inc. (incorporated by reference to Exhibit 3.1 to the Form 8-K filed on September 10, 2018)

3.9

Certificate of Designation of Preferences, Rights and Limitations of Series D Convertible Preferred Stock (incorporated by reference to Exhibit 3.1 to the Form 8-K filed on November 9, 2017)

3.10

Certificate of Designation of Preferences, Rights and Limitations of Series E Convertible Preferred Stock (incorporated by reference to Exhibit 3.1 to the Form 8-K filed on February 16, 2018)

3.11

Certificate of Designations of Series F Junior Participating Preferred Stock of BioSig Technologies, Inc. (incorporated by reference to Exhibit 3.1 to the Form 8-K filed on July 17, 2020)

3.12

Amended and Restated Bylaws of BioSig Technologies, Inc. (incorporated by reference to the Exhibit 3.1 to the Form 8-K filed on September 27, 2019)

3.13

Amendment No. 1 to Amended and Restated Bylaws of BioSig Technologies, Inc. (incorporated by reference to Exhibit 3.1 to the Form 8-K filed on October 22, 2019)

4.1

Form of Warrant (incorporated by reference to the Exhibit 4.1 to the Form 8-K filed on March 24, 2022)

4.2

Form of Underwriter Warrant (incorporated by reference to the Exhibit 4.1 to the Form 8-K filed on June 29, 2022)

10.1

Form of Securities Purchase Agreement (incorporated by reference to the Exhibit 10.1 to the Form 8-K filed on March 24, 2022)

31.01*

Certification of Chief Executive Officer pursuant to Exchange Act Rules 13a-14(a) and 15d-14(a), as adopted pursuant to Section 302 of the Sarbanes-Oxley Act of 2002.

31.02*

31.02

32.01*

32.01

101 INS*

101 INS

Inline XBRL Instance Document

101 SCH*

101 SCH

Inline XBRL Taxonomy Extension Schema Document

101 CAL*

101 CAL

Inline XBRL Taxonomy Calculation Linkbase Document

101 DEF*

101 DEF

Inline XBRL Taxonomy Extension Definition Linkbase Document

101 LAB*

101 LAB

Inline XBRL Taxonomy Labels Linkbase Document

101 PRE*

101 PRE

Inline XBRL Taxonomy Presentation Linkbase Document

104*

Cover Page Interactive Data File (formatted as Inline XBRL and contained in Exhibit 101)



* Filed herewith.




SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized.

BIOSIG TECHNOLOGIES, INC.

Date: November 9, 2017August 15, 2022

By:

/s/ KENNETH L. LONDONER

Kenneth L. Londoner

Kenneth L. Londoner

Chairman & Chief Executive Officer (Principal Executive Officer)

Date: November 9, 2017August 15, 2022

By:

/s/ STEVEN CHAUSSYSteven Chaussy

Steven Chaussy

Chief Financial Officer (Principal Accounting Officer)



43



 
36iso4217:USD xbrli:shares