UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

WASHINGTON, D.C. 20549

 

FORM 10-Q

(Mark One)

 

QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

 

For the quarterly period ended September 30, 20222023

or

 

TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

 

For the transition period from _____to _____

 

Commission File Number 001-39825

 

Intelligent Bio Solutions Inc.

(Exact name of Registrant as specified in its Charter)

 

Delaware 82-1512711

(State or other jurisdiction of

(I.R.S. Employer
incorporation or organization)

 

(I.R.S. Employer

Identification No.)

Intelligent Bio Solutions Inc.,

142 West, 57th 57th Street, 11th Floor, New York, NY

 10019
(Address of principal executive offices) (Zip Code)

 

Registrant’s telephone number, including area code: (646) 828-8258

 

Securities registered pursuant to Section 12(b) of the Act:

 

Title of each class Trading Symbol(s) Name of each exchange on which registered
Common Stock, par value $0.01 per share INBS The Nasdaq Stock Market LLC

 

Securities registered pursuant to Section 12(g) of the Act: None

 

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 every Interactive Data File required to be submitted pursuant to Rule 405 of Regulation S-T (§232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit 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 the definitions of “large accelerated filer,”filer”, “accelerated filer,” “smaller reporting company,” and “emerging growth company” in Rule 12b-2 of the Exchange Act.

 

Large accelerated filerAccelerated filer
Non-accelerated filerSmaller 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 Act). YES ☐ NO

 

As of November 10, 2022,3, 2023, there were 18,352,9958,734,381 shares of the registrant’s Common Stock issued and outstanding.

 

 

 

 
 

Table of Contents

 

 Page
PART I.FINANCIAL INFORMATION3
Item 1.Financial Statements (unaudited)3
 Condensed Consolidated Balance Sheets3
 Condensed Consolidated Statements of Operations and Other Comprehensive Loss4
 Condensed Consolidated Statements of Changes in Shareholders’ Equity5
 Condensed Consolidated Statements of Cash Flows6
 Notes to Condensed Consolidated Financial Statements7
Item 2.Management’s Discussion and Analysis of Financial Condition and Results of Operations.1725
Item 3.Quantitative and Qualitative Disclosures About Market Risk.2431
Item 4.Controls and Procedures.2431
  
PART II.OTHER INFORMATION33
Item 1.Legal Proceedings.2633
Item 1A.Risk Factors.2633
Item 2.Unregistered Sales of Equity Securities and Use of Proceeds.2734
Item 3.Defaults Upon Senior Securities.2734
Item 4.Mine Safety Disclosures.2734
Item 5.Other Information.2734
Item 6.Exhibits.2835
Signatures29
36

2

 

PART I. FINANCIAL INFORMATION

ITEM 1. FINANCIAL STATEMENTS

Intelligent Bio Solutions Inc.

Condensed Consolidated Balance Sheets

 

  September 30, 2022 (Unaudited)  June 30, 2022 
ASSETS        
Current assets:        
Cash and cash equivalents $5,742,626  $8,238,301 
Deferred charges  300,000   - 
Grant receivable, current portion  1,443,939   1,529,882 
Research and development tax incentive receivable  571,860   353,048 
Other current assets  148,927   746,761 
Total current assets  8,207,352   10,867,992 
Long-term grant receivable  1,031,384   1,092,773 
Construction in progress  416,029   391,408 
Other non-current assets  504,938   - 
TOTAL ASSETS $10,159,703  $12,352,173 
         
LIABILITIES AND SHAREHOLDERS’ EQUITY        
Current liabilities:        
Accounts payable and accrued expenses $1,038,545  $1,625,089 
Current portion of deferred grant income  1,018,918   2,836,582 
Current employee benefit liabilities  299,686   201,332 
Total current liabilities  2,357,149   4,663,003 
Employee benefit liabilities  20,791   50,626 
Long-term deferred grant income  2,585,629   1,092,773 
Total liabilities  4,963,569   5,806,402 
Commitments and contingencies (Note 11)  -   - 
         
Shareholders’ equity:        
Common stock, $0.01 par value, 100,000,000 shares authorized, 14,889,904 shares issued and outstanding at September 30, 2022 and June 30, 2022, respectively  148,899   148,899 
Additional paid-in capital  38,440,011   38,440,011 
Accumulated deficit  (32,384,146)  (31,175,853)
Accumulated other comprehensive loss  (923,694)  (788,135)
Total consolidated Intelligent Bio Solutions Inc. equity  5,281,070   6,624,922 
Non-controlling interest  (84,936)  (79,151)
Total shareholders’ equity  5,196,134   6,545,771 
TOTAL LIABILITIES AND SHAREHOLDERS’ EQUITY $10,159,703  $12,352,173 

The accompanying notes are an integral part of these unaudited condensed consolidated financial statements.

Intelligent Bio Solutions Inc.

Condensed Consolidated Statements of Operations and Other Comprehensive Loss

(Unaudited)

  2022  2021 
  Three Months Ended September 30, 
  2022  2021 
Revenue:  -   - 
Other income:        
Government support income $311,320  $- 
Total revenue and other income  311,320   - 
         
Operating expenses:        
General and administrative expenses  1,450,418   1,332,520 
Development and regulatory approval expenses  79,274   106,799 
Total operating expenses  1,529,692   1,439,319 
Loss from operations  (1,218,372)  (1,439,319)
         
Other income (expense):        
Interest expense  (1,065)  - 
Realized foreign exchange loss  (2,247)  (3,118)
Interest income  7,606   4,597 
Total other income (expense)  4,294   1,479 
Net loss  (1,214,078)  (1,437,840)
Net loss attributable to non-controlling interest  (5,785)  (5,188)
Net loss attributable to Intelligent Bio Solutions Inc. $(1,208,293) $(1,432,652)
         
Other comprehensive loss, net of tax:        
Foreign currency translation loss $(135,559) $(67,482)
Total other comprehensive loss  (135,559)  (67,482)
Comprehensive loss  (1,349,637)  (1,505,322)
Comprehensive loss attributable to non-controlling interest  (5,785)  (5,188)
Comprehensive loss attributable to Intelligent Bio Solutions Inc. $(1,343,852) $(1,500,134)
         
Net loss per share, basic and diluted $(0.08) $(0.10)
Weighted average shares outstanding, basic and diluted  14,889,904   14,006,127 

The accompanying notes are an integral part of these unaudited condensed consolidated financial statements.

   September 30, 2023
(Unaudited)
   June 30, 2023 
ASSETS        
Current assets:        
Cash and cash equivalents $186,401  $1,537,244 
Accounts receivable, net  567,510   293,861 
Inventories, net  965,091   979,907 
Research and development tax incentive receivable  559,588   498,758 
Other current assets  413,305   552,791 
Total current assets  2,691,895   3,862,561 
Property and equipment, net  664,922   690,175 
Operating lease right-of-use assets  471,532   546,475 
Intangible assets, net  4,872,141   5,255,401 
TOTAL ASSETS $8,700,490  $10,354,612 
         
LIABILITIES AND SHAREHOLDERS’ EQUITY        
Current liabilities:        
Accounts payable and accrued expenses $3,628,797  $2,610,028 
Current portion of operating lease liabilities  227,414   223,447 
Current portion of deferred grant income  2,240,929   2,338,057 
Current employee benefit liabilities  406,964   358,942 
Current portion of notes payable  341,834   353,211 
Total current liabilities  6,845,938   5,883,685 
Employee benefit liabilities, less current portion  27,732   24,902 
Operating lease liabilities, less current portion  284,028   356,165 
Notes payable, less current portion  306,234   402,862 
Total liabilities  7,463,932   6,667,614 
Commitments and contingencies (Note 13)  -    
         
Shareholders’ equity:        
Common stock, $0.01 par value, 100,000,000 shares authorized, 2,330,399 shares issued and outstanding at September 30, 2023 and June 30, 2023, respectively  23,304   23,304 
Treasury stock, at cost, 1,386 shares as of September 30, 2023 and June 30, 2023, respectively  (14)  (14)
Additional paid-in capital  46,158,763   46,158,763 
Accumulated deficit  (44,232,777)  (41,807,573)
Accumulated other comprehensive loss  (593,512)  (575,496)
Total consolidated Intelligent Bio Solutions Inc. equity  1,355,764   3,798,984 
Non-controlling interest  (119,206)  (111,986)
Total shareholders’ equity  1,236,558   3,686,998 
TOTAL LIABILITIES AND SHAREHOLDERS’ EQUITY $8,700,490  $10,354,612 

 

4

Intelligent Bio Solutions Inc.

Condensed Consolidated Statements of Changes in Shareholders’ Equity

(Unaudited)

  Shares  Amount  Shares  Amount  capital  deficit  loss  interest  (deficit) 
                          Total 
  Preferred stock  Common stock  Additional
paid in
  Accumulated  Other
comprehensive
  Non-
controlling
  shareholders’
equity
 
  Shares  Amount  Shares  Amount  capital  deficit  loss  interest  (deficit) 
Balance, June 30, 2022  -  $-   14,889,904  $148,899  $38,440,011  $(31,175,853) $(788,135) $(79,151) $6,545,771 
Foreign currency translation loss  -   -   -   -   -   -   (135,559)  -   (135,559)
Net loss  -   -   -   -   -   (1,208,293)  -   (5,785)  (1,214,078)
Balance, September 30, 2022  -  $-   14,889,904  $148,899  $38,440,011  $(32,384,146) $(923,694) $(84,936) $5,196,134 
                                     
Balance, June 30, 2021  1,300,000  $13,000   13,582,122  $135,821  $38,440,089  $(22,869,803) $(661,260) $(51,226) $15,006,621 
Balance  1,300,000  $13,000   13,582,122  $135,821  $38,440,089  $(22,869,803) $(661,260) $(51,226) $15,006,621 
Series B warrants exercised to purchase common shares  -   -   400   4   (4)  -   -   -   - 
Conversion of convertible preferred shares into common shares  (1,300,000)  (13,000)  1,300,000   13,000   -   -   -   -   - 
Foreign currency translation loss  -   -   -   -   -   -   (67,482)  -   (67,482)
Net loss  -   -   -   -   -   (1,432,652)  -   (5,188)  (1,437,840)
Balance, September 30, 2021  -  $-   14,882,522  $148,825  $38,440,085  $(24,302,455) $(728,742) $(56,414) $13,501,299 
Balance  -  $-   14,882,522  $148,825  $38,440,085  $(24,302,455) $(728,742) $(56,414) $13,501,299 

The accompanying notes are an integral part of these unaudited condensed consolidated financial statements.

 

53

Intelligent Bio Solutions Inc.

Condensed Consolidated Statements of Operations and Other Comprehensive Loss*

(Unaudited)

       
  Three Months Ended September 30, 
  2023  2022 
Revenue $796,094  $- 
Cost of revenue (exclusive of amortization shown separately below)  (563,763)  - 
Gross profit  232,331   - 
         
Other income:        
Government support income  109,871   311,320 
         
Operating expenses:        
Selling, general and administrative expenses  (2,457,060)  (1,450,418)
Development and regulatory approval expenses  (103,947)  (79,274)
Depreciation and amortization  (307,560)  - 
Total operating expenses  (2,868,567)  (1,529,692)
Loss from operations  (2,526,365)  (1,218,372)
         
Other income (expense):        
Interest expense  (37,448)  (1,065)
Realized foreign exchange loss  -   (2,247)
Fair value gain on revaluation of financial instrument  131,250   - 
Interest income  139   7,606 
Total other income  93,941   4,294 
Net loss  (2,432,424)  (1,214,078)
Net loss attributable to non-controlling interest  (7,220)  (5,785)
Net loss attributable to Intelligent Bio Solutions Inc. $(2,425,204) $(1,208,293)
         
Other comprehensive loss, net of tax:        
Foreign currency translation loss $(18,016) $(135,559)
Total other comprehensive loss  (18,016)  (135,559)
Comprehensive loss  (2,450,440)  (1,349,637)
Comprehensive loss attributable to non-controlling interest  (7,220)  (5,785)
Comprehensive loss attributable to Intelligent Bio Solutions Inc. $(2,443,220) $(1,343,852)
         
Net loss per share, basic and diluted* $(1.04) $(1.62)
Weighted average shares outstanding, basic and diluted*  2,330,399   744,495 

 

Intelligent Bio Solutions Inc.

Condensed Consolidated Statements of Cash Flows

(Unaudited)

  2022  2021 
  Three Months Ended September 30, 
  2022  2021 
Cash flows from operating activities:        
Net loss $(1,214,078) $(1,437,840)
Adjustments to reconcile net loss to net cash used in operating activities:        
Loss/ (gain) on foreign currency translation, net  2,247   3,118 
Non-cash refund of R&D expenditure claims  (60,413)  - 
Non-cash other operating activities  25,035   20,136 
Changes in assets and liabilities:        
Grant receivable, current and non-current  147,332   2,503,875 
Research and development tax incentive receivable, current  (218,812)  - 
Deferred charges  (300,000)  - 
Other assets, current and non-current  92,896   240,246 
Accounts and other payables  (13,299)  (635,568)
Accounts payable - related party  -   55,485 
Deferred grant income, current and non-current  (324,808)  (674,984)
Other long-term liabilities  (29,835)  8,494 
Net cash (used in) provided by operating activities  (1,893,735)  82,962 
Cash flows from investing activities:        
Amount invested on construction in progress  (474,891)  - 
Net cash used in investing activities  (474,891)  - 
         
Effect of foreign exchange rates on cash and cash equivalents  (127,049)  (48,179)
         
(Decrease) increase in cash and cash equivalents  (2,495,675)  34,783 
Cash and cash equivalents, beginning of period  8,238,301   12,573,685 
Cash and cash equivalents, end of period $5,742,626  $12,608,468 
         
Non-cash investing and financing activities        
Conversion of preferred shares into common shares $-  $13,000 

The accompanying notes are an integral part of these unaudited condensed consolidated financial statements.

*Common Stock and per share amount have been retroactively adjusted to reflect the decreased number of shares resulting from a 1 for 20 reverse stock split effected on February 9, 2023, throughout the condensed consolidated financial statement unless otherwise stated.

4

Intelligent Bio Solutions Inc.

Condensed Consolidated Statements of Changes in Shareholders’ Equity*

(Unaudited)

 

                            
  Common stock  Treasury stock  Additional     Other  Non-  Total 
  Shares  Amount  Shares  Amount  paid in capital  Accumulated
deficit
  comprehensive
loss
  controlling
interest
  shareholders’
equity
 
Balance, June 30, 2023*  2,330,399  $23,304   (1,386) $(14) $46,158,763  $(41,807,573) $(575,496) $(111,986) $3,686,998 
Foreign currency translation loss*  -   -   -   -   -   -   (18,016)  -   (18,016)
Net loss*  -   -   -   -   -   (2,425,204)  -   (7,220)  (2,432,424)
Balance, September 30, 2023*  2,330,399  $23,304   (1,386) $(14) $46,158,763  $(44,232,777) $(593,512) $(119,206) $1,236,558 
                                     
Balance, June 30, 2022*  744,495  $7,445   -  $-  $38,581,465  $(31,175,853) $(788,135) $(79,151) $6,545,771 
Balance  744,495  $7,445   -  $-  $38,581,465  $(31,175,853) $(788,135) $(79,151) $6,545,771 
Foreign currency translation loss*  -   -   -   -   -   -   (135,559)  -   (135,559)
Net loss*  -   -   -   -   -   (1,208,293)  -   (5,785)  (1,214,078)
Balance, September 30, 2022*  744,495  $7,445   -  $-  $38,581,465  $(32,384,146) $(923,694) $(84,936) $5,196,134 
Balance  744,495  $7,445   -  $-  $38,581,465  $(32,384,146) $(923,694) $(84,936) $5,196,134 

The accompanying notes are an integral part of these unaudited condensed consolidated financial statements.

*Common Stock and per share amount have been retroactively adjusted to reflect the decreased number of shares resulting from a 1 for 20 reverse stock split effected on February 9, 2023, throughout the condensed consolidated financial statement unless otherwise stated.

5

Intelligent Bio Solutions Inc.

Condensed Consolidated Statements of Cash Flows

(Unaudited)

       
  Three Months Ended September 30, 
  2023  2022 
Cash flows from operating activities:        
Net loss $(2,432,424) $(1,214,078)
Adjustments to reconcile net loss to net cash used in operating activities:        
Depreciation and amortization  247,598   - 
Amortization of right-of-use assets  59,962   - 
Non-cash loss on foreign currency translation, net  -   2,247 
Provision for inventory obsolescence  67,851   - 
Non-cash refund of R&D expenditure claims  (33,523)  (60,413)
Fair value gain on revaluation of holdback Series C preferred stock  (131,250)  - 
Non-cash other operating activities  104,485   25,035 
Changes in operating assets and liabilities:        
Accounts receivable  (273,649)  - 
Inventories  (53,035)  - 
Grant receivable / deferred grant income  (97,128)  (177,476)
Research and development tax incentive receivable  (60,830)  (218,812)
Other current assets  139,486   (207,104)
Accounts and other payables  1,215,964   (13,299)
Operating lease liabilities  (68,170)  - 
Other long-term liabilities  2,830   (29,835)
Net cash used in operating activities  (1,311,833)  (1,893,735)
Cash flows from investing activities:        
Amount invested on construction in progress  -   (474,891)
Net cash used in investing activities  -   (474,891)
         
Effect of foreign exchange rates on cash and cash equivalents  (39,010)  (127,049)
         
Decrease in cash and cash equivalents  (1,350,843)  (2,495,675)
Cash and cash equivalents, beginning of period  1,537,244   8,238,301 
Cash and cash equivalents, end of period $186,401  $5,742,626 

The accompanying notes are an integral part of these unaudited condensed consolidated financial statements.

6

Intelligent Bio Solutions Inc.

Notes to the Condensed Consolidated Financial Statements

(Unaudited)

NOTE 1. ORGANIZATION AND DESCRIPTION OF THE BUSINESS

Business

Intelligent Bio Solutions Inc. (formerly known as GBS Inc.) (“INBS”), and its wholly owned Delaware subsidiary, GBS Operations Inc. were each formed on December 5, 2016, under the laws of the state of Delaware. Our Australian subsidiary Intelligent Bio Solutions (APAC) Pty Ltd (formerly known as Glucose Biosensor Systems (Greater China) Pty LtdLtd) was formed on August 4, 2016, under the laws of New South Wales, Australia and was renamed to GBSIntelligent Bio Solutions (APAC) Pty Ltd on October 14, 2020. Glucose Biosensor Systems (Japan) Pty Ltd and Glucose Biosensor Systems (APAC) Pty Ltd were formed under the laws of New South Wales, Australia on February 22, 2017 and February 23, 2017 respectively.January 6, 2023. On October 26,4, 2022, the Company changed its corporate nameINBS acquired Intelligent Fingerprinting Limited (“IFP”), a company registered in England and Wales (the “Name Change”“IFP Acquisition”) from “GBS Inc.” to “Intelligent Bio Solutions Inc.” For purpose of the Quarterly Report on Form 10-Q, the terms “Company”, “we,” “us” and “our” refer to. INBS and its consolidated subsidiaries (collectively, “we,” “us,” “our,” “INBS” or the “Company,” unless context requires or indicates otherwise.otherwise) were formed to provide a non-invasive, pain free innovative medical devices and screening devices. Our headquarters are in New York, New York.

 

We are a medical technology company operating acrossfocused on developing and delivering intelligent, rapid, non-invasive testing and screening solutions. We operate globally with the Asia-Pacific region (the “APAC Region”) with an objective to introduceof providing innovative and deliver intelligent pain free diagnostic tests. We also have an interest inaccessible solutions that improve the North America region. Our goal is to expand the global footprintquality of our drug screening tests following our recent acquisition of Intelligent Fingerprinting Limited, while continuing to develop our Biosensor Platform that we license from Life Science Biosensor Diagnostics Pty Ltd (“LSBD” or the “Licensor”). This will be followed by developing both of our platforms to their full capacity across multiple diagnostic modalities of immunology, hormones, chemistry, tumor markers and nucleic acid tests.life.

Reverse Stock Split

 

On February 9, 2023, the Company filed a certificate of amendment (the “Certificate of Amendment”) to its amended and restated certificate of incorporation to effect, as of February 9, 2023, a 1-for-20 reverse split of the Company’s common stock (the “Reverse Stock Split”).

7

NOTE 2. LIQUIDITY AND GOING CONCERN

The Financial Accounting Standards Board (“FASB”) Accounting Standards Codification (“ASC”) Topic 205-40, Presentation of Financial Statements - Going Concern (ASC 205-40) requires management to assess an entity’s ability to continue as a going concern within one year of the date of the financial statements are issued. In each reporting period, including interim periods, an entity is required to assess conditions known and reasonably knowable as of the financial statement issuance date to determine whether it is probable an entity will not meet its financial obligations within one year from the financial statement issuance date. Substantial doubt about an entity’s ability to continue as a going concern exists when conditions and events, considered in the aggregate, indicate it is probable the entity will be unable to meet its financial obligations as they become due within one year after the date the financial statements are issued.

The Company is an emerging growth company and has not generated any revenues to date. As such, the Company is subject to all of the risks associated with emerging growth companies. Since inception, the Company has incurred losses and negative cash flows from operating activities. The Company does not expect to generate positive cash flows from operating activities in the near future until such time, if at all, the Company completes the development process of its products, including regulatory approvals, and thereafter, begins to commercialize and achieve substantial acceptance in the marketplace for the first of a series of products in its medical device portfolio.

 

The Company incurred a net losses of $2,425,204 (after losses attributable to non-controlling interest) for the three months ended September 30, 2023 (net loss of $1,208,293 for the three months ended September 30, 2022 (net loss2022). As of $1,432,652 for the three months ended September 30, 2021). At September 30, 2022,2023, the Company has shareholders’ equity of $5,196,1341,236,558, a working capital deficit of $5,850,2034,154,043, and an accumulated deficit of $32,384,14644,232,777.

 

In the near future, theThe Company anticipates incurring operating losses andfor the foreseeable future. The Company does not expect to experiencegenerate positive cash flows from operating activities and may continue to incur operating losses until it completes the development of its products and seeksseek regulatory approvals to market such products.

 

The Company has evaluated whether there are conditions and events, considered in the aggregate, that raise a substantial doubt about its ability to continue as going concern within one year after the date of release of the unaudited condensed consolidated financial statements. The Company expects that its cash and cash equivalents as of September 30, 2022,2023, of $5,742,626186,401, maywill be insufficient to allow the Company to fund its current operating plan through at least the next twelve months from the issuance of these unaudited condensed consolidated financial statements, taking into account the acquisition of Intelligent Fingerprinting Limited. Should revenue not be generated during this period to cover expenses, then thesestatements. These conditions may raise substantial doubt about the Company’s ability to continue as a going concern for a period of at least one year from the date these unaudited condensed consolidated financial statements are issued. Accordingly, it appears that the Company will be required to raise additional funds during the next 12 months. The Company is currently evaluating potentially raising additional funds through private placements and/or public equity financing. However, there can be no assurance that in the event thatwhen the Company requires additional financing, such financing will be available on terms which are favorable to the Company, or at all. If the Company is unable to raise additional funding to meet its working capital needs in the future, it will be forced to delay or reduce the scope of its research programs and/or limit or cease its operations. In addition, the Company may be unable to realize its assets and discharge its liabilities in the normal course of business.

Accordingly, these factors raise substantial doubt about the Company’s ability to continue as a going concern unless it can successfully raise additional capital.

 

7

On October 4, 2023, subsequent to the quarter ended September 30, 2023, the Company raised approximately $4.378 million prior to deducting underwriting discounts and commissions and offering expenses via a registered underwritten public offering of the Company’s securities. Net proceeds to the Company, after deducting the underwriting discounts and commissions and estimated offering expenses payable by the Company, were approximately $3.35 million. Refer to Note 15 for details.

The Company’s unaudited condensed consolidated financial statements have been prepared on a going concern basis which contemplates the realization of assets and satisfaction of liabilities and commitments in the normal course of business. The unaudited condensed consolidated financial statements do not include any adjustments relating to the recoverability and classification of recorded asset amounts or the amounts and classification of liabilities should the Company be unable to continue as a going concern.

NOTE 3. SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES

Basis of presentation

 

The unaudited condensed consolidated financial statements of the Company have been prepared in accordance with accounting principles generally accepted in the United States of America (“GAAP”) for interim financial information and the instructions to Form 10-Q and Article 10 of Regulation S-X. Accordingly, our unaudited condensed consolidated financial statements do not include all the information and footnotes required by GAAP for complete financial statements. Normal and recurring adjustments considered necessary for a fair statement of the results for the interim periods, in the opinion of the Company’s management, have been included. Operating results for the three months ended September 30, 2022,2023, are not necessarily indicative of the results that may be expected for the year ending June 30, 2023.2024. The accompanying unaudited condensed consolidated financial statements and related footnote disclosures should be read in conjunction with the consolidated financial statements and notes thereto included in our Form 10-K and 10-K/A for the fiscal year ended June 30, 2022,2023, which was filed with the U.S. Securities and Exchange Commission (the “SEC”) on September 22, 2022 and amended on Form 10-K/A filed with the SEC on October 7, 2022 (as amended, the “2022August 23, 2023 (the “2023 Form 10-K”).

 

The unaudited condensed consolidated financial statements and notes thereto give retrospective effect to the Reverse Stock Split for all periods presented. All common stock, options exercisable for common stock, restricted stock units, warrants and per share amounts contained in the unaudited condensed consolidated financial statements have been retrospectively adjusted to reflect the Reverse Stock Split for all periods presented.

8

Principles of consolidation

 

These unaudited condensed consolidated financial statements include the accounts of the Company, all wholly owned and majority-owned subsidiaries in which the Company has a controlling voting interest and, when applicable, variable interest entities in which the Company has a controlling financial interest or is the primary beneficiary. Investments in affiliates where the Company does not exert a controlling financial interest are not consolidated.consolidated.

 

All significant intercompany transactions and balances have been eliminated upon consolidation.

 

Equity offering costs

 

The Company complies with the requirements of Accounting Standards Codification (“ASC 340,340”), Other Assets and Deferred Costs, with regards to offering costs. Prior to the completion of an offering, offering costs are capitalized as deferred offering costs on the consolidated balance sheets. The deferred offering costs will be charged to shareholders’ equity upon the completion of the relatedan offering.

 

Use of estimates

 

The preparation of consolidated financial statements in conformity with GAAP requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the consolidated financial statements, and the reported amounts of revenue and expenses during the reporting period. Actual results could materially differ from those estimates.

 

8

Business combinations

Revenue recognition

 

The results of businesses acquired in a business combination are included in the Company’s consolidated financial statements from the date of the acquisition. The Company uses the acquisition method of accounting and allocates the purchase price to the identifiable assets and liabilities of the relevant acquired business at their acquisition date fair values. Any excess consideration over the fair value of assets acquired and liabilities assumed is recognized as goodwill. The allocation of the purchase price in a business combination requires the Company to perform valuations with significant judgment and estimates, including the selection of valuation methodologies, estimates of future revenue, costs and cash flows, discount rates and selection of comparable companies. The Company engages the assistance of valuation specialists in concluding on fair value measurements in connection with determining fair values of assets acquired and liabilities assumed in a business combination. As a result, during the measurement period, which may be up to one year from the acquisition date, the Company records adjustments to the assets acquired and liabilities assumed with the corresponding offset to goodwill. Upon the conclusion of the measurement period or final determination of the values of assets acquired or liabilities assumed, whichever comes first, any subsequent adjustments are recorded to the consolidated statements of operations. Transaction costs associated with business combinations are expensed as incurred and are included in selling, general and administrative expense in the consolidated statements of operations.

Revenue recognition

Revenue is accounted for under ASC 606 Revenue from Contracts with Customers through the following steps:

Identify the contract with a customer;
Identify the performance obligations in the contract;
Determine the transaction price;
Allocate the transaction price to performance obligations in the contract; and
Recognize revenue when or as the Company satisfies a performance obligation.

The Company recognized revenue from contracts with customers is recognized when, or as, the Companyit satisfies its performance obligations by delivering the promised goods or service deliverables to the customers. A good or service deliverable is transferred to a customer when, or as, the customer obtains control of that good or service deliverable.

 

9

Deferred grantFinancial information presented on a consolidated basis accompanied by disaggregated information about revenue and other income by product types for the purpose of allocating resources and evaluating financial performance. Currently, the Company has two products offerings. Accordingly, the Company has determined the following reporting segments (refer to Note 4, Segment Information):

 

1)Commercially available Intelligent Fingerprinting Products (IFPG)
2)Development Stage Saliva Glucose Biosensor Platform (SGBP)

Revenues are used to evaluate the performance of the Company’s segments, the progress of major initiatives and the allocation of resources. All of the Company’s revenues are attributable to the IFPG segment during the quarter ended September 30, 2023. There were no revenues during the three months ended September 30, 2022.

Revenue from the IFPG segment relates to the sale of readers, cartridges and accessories and is summarized as follows:

SCHEDULE OF REVENUE SALES OF READERS CARTRIDGES AND ACCESSORIES

       
  Three Months Ended September 30, 
  2023  2022 
Sales of goods - cartridges $380,059  $ 
Sales of goods - readers  238,802    
Other sales  177,233    
Total revenue $796,094  $ 

Other income

The other income is mainly comprised of grant income and research and development (“R&D”) tax refund.

a) Grant income

On June 30, 2021, the Company executed a definitive grant agreement with the Australian Government to assist with building a manufacturing facility. The grant has a total value of up to $4.7 million upon the achievement of certain milestones until March 28, 2024. Proceeds from the grant will be used primarily to reimburse the Company for costs incurred in the construction of the manufacturing facility.

 

Accounting for the grant does not fall under ASC 606, Revenue from Contracts with Customers, as the Australian Government will not benefit directly from our manufacturing facility. As there is no authoritative guidance under U.S. GAAP on accounting for grants to for-profit business entities, we applied International Accounting Standards 20 (“IAS 20”), Accounting for Government Grants and Disclosure of Government Assistance by analogy when accounting for the Australian Government grant to the Company. Furthermore, disclosures made below are in accordance with the disclosure requirements of Accounting Standards Update (“ASU”) 2021-10 (see recently issued accounting pronouncements below for more information).

 

The Australian Government grant proceeds, which will be used to reimburse construction costs incurred, meet the definition of grants related to assets as the primary purpose for the payments is to fund the construction of a capital asset. Under IAS 20, government grants related to assets are presented in the statement of financial position either by setting up the grant as deferred income that is recognized in the statement of operation on a systematic basis over the useful life of the asset or by deducting the grant in arriving at the carrying amount of the asset. Either of these two methods of presentation of grants related to assets in financial statements are regarded as acceptable alternatives under IAS 20. The Company has elected to record the grants received initially as deferred income and deducting the grant proceeds received from the gross costs of the assets or construction in progress (“CIP”) and the deferred grant income liability. A total of $629,354 and $646,116 was recognized as a reduction to the CIP asset on the consolidated balance sheets as of September 30, 2023 and June 30, 2023, respectively.

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Under IAS 20, government grants are initially recognized when there is reasonable assurance the conditions of the grant will be met, and the grant will be received. As of June 30, 2021, management concluded that there was reasonable assurance the grant conditions will be met, and all milestone payment received. The total grant value of $4.7 million was recognized as both a grant receivable and deferred grant income on the grant effective date. The project has been delayed due to global shortages of semiconductors that are used in manufacturing equipment and global supply chain disruption due to the coronavirus pandemic in the preceding year. The Company has only completed 4 of the 8 milestones in the grant agreement. As of September 30, 2023, there was uncertainty regarding the potential extension of the grant agreement past its original end of March 28, 2024. Therefore, management concluded that there was no reasonable assurance that the remaining grant receivable was reduced by $2.1 million for payments received during the twelve months ended June 30, 2022 (no payments were received during the three months ended September 30, 2022) and $2.5 million remains in grant receivable on the Condensed Consolidated Balance Sheets for the period ended September 30, 2022. The receivable balance at September 30, 2022 is arrived at after considering the forex impact on the grant receivable by foreign subsidiary.will be received.

 

After initial recognition, under IAS 20, government grants are recognized in earnings on a systematic basis in a manner that mirrors the manner in which the Company recognizes the underlying costs for which the grant is intended to compensate. Further, IAS 20 permits for recognition in earnings either separately under a general heading such as other income, or as a reduction of the cost of the asset. The Company has elected to recognize government grant income separately within other income for operating expenditures. Similarly, for capital expenditures, the carrying amount of assets purchased or constructed out of the grant funds are presented net by deducting the grant proceeds received from the gross costs of the assets or CIP and deferred grant income liability. A total of $33,523 and $60,413 deferred grant income was recognized within other income during the current period.three months ended September 30, 2023 and 2022, respectively.

 

b) R&D tax refund

The Company measures the R&D grant income and receivable by considering the time spent by employees on eligible R&D activities and R&D costs incurred to external service providers. The R&D tax refund receivable is recognized as the Company believes that it is probable that the amount will be recovered in full through a future claim. A total of $76,348 and $250,907 of R&D tax refund income is recognized in other income during the three months ended September 30, 2023, and 2022, respectively.

Development and regulatory approval costsexpenses

 

Expenditures relating to research and development (“R&D”)&D are expensed as incurred and recorded in development and regulatory approval in the Condensed Consolidated Statementscondensed consolidated statements of Operationsoperations and Other Comprehensive Loss. R&D expenses include external expenses incurred under arrangements with third parties; salaries and personnel-related costs; license fees to acquire in-process technology and other expenses. The Company recognizes the benefit of refundable R&D tax refunds as a R&D tax refund income when there is reasonable assurance that the amount claimed will be recovered (refer to the R&D tax refund discussion below)above).

9

 

Intellectual property acquired for a particular research and development project and that have no alternative future uses (in other research and development projects or otherwise) are expensed in research and development costs at the time the costs are incurred.

 

In certain circumstances, the Company may be required to make advance payments to vendors for goods or services that will be received in the future for use in R&D activities. In such circumstances, the non-refundable advance payments are deferred and capitalized, even when there is no alternative future use for the R&D, until the related goods or services are provided. In circumstances where amounts have been paid in excess of costs incurred, the Company records a prepaid expense.

 

R&D tax refund

The Company measures the R&D grant income and receivable by considering the time spent by employees on eligible R&D activities and R&D costs incurred to external service providers. The R&D tax refund receivable is recognized as the Company believes that it is probable that the amount will be recovered in full through a future claim. A total of $250,907 and $nil of R&D tax refund income was recognized in other income during the three months ended September 30, 2022, and 2021, respectively.

Foreign currency translation

 

Assets and liabilities of foreign subsidiaries are translated from local (functional) currency to reporting currency (U.S. dollar) at the spot rate of exchange in effect on the consolidated balance sheets date; income and expenses are translated at the average rate of exchange prevailing during the year. The functional currency of INBS is the United States dollar. Foreign currency movements resulted in a loss of $135,55918,016 and $67,482135,559 for the three months ended September 30, 2022,2023 and 2021,2022, respectively.

 

11

Income taxes

 

In accordance with the provisions of FASBthe Financial Accounting Standards Board (“FASB”) ASC 740, Income Taxes, tax positions initially need to be recognized in the consolidated financial statements when it is more likely than not that the positions will be sustained upon examination by taxing authorities. It also provides guidance for de-recognition, classification, interest and penalties, accounting in interim periods, disclosure, and transition.

 

As of September 30, 2022,2023, the Company had no uncertain tax positions that qualified for either recognition or disclosure in the unaudited condensed consolidated financial statements. Additionally, the Company had no interest and penalties related to income taxes.

 

The Company accounts for current and deferred income taxes and, when appropriate, deferred tax assets and liabilities are recorded with respect to temporary differences in the accounting treatment of items for financial reporting purposes and for income tax purposes. Where, based on the weight of all available evidence, it is more likely than not that some amount of the recorded deferred tax assets will not be realized, a valuation allowance is established for that amount that, in management’s judgment, is sufficient to reduce the deferred tax asset to an amount that is more likely than not to be realized.

Licensing rights

Cash and Cash equivalent

The Company considers all highly liquid investments with a maturity of 90 days or less at the time of purchase to be cash equivalents. The carrying values of cash and cash equivalents approximate their fair values due to the short-term nature of these instruments. As of September 30, 2023 and June 30, 2023, there were no cash equivalents. The Company maintains cash accounts with financial institutions. At times, balances in these accounts may exceed federally insured limits. The amounts over these insured limits as of September 30, 2023, and June 30, 2023, was $0 and $1,114,687, respectively. No losses have been incurred to date on any deposits.

Inventories

Inventories are stated at the lower of cost or net realizable value. Cost comprises direct materials and, where applicable, other costs that have been incurred in bringing the inventories to their present location and condition. Net realizable value is the estimated selling price less all estimated costs of completion and costs to be incurred in marketing, selling and distribution. General market conditions, as well as the Company’s research activities, can cause certain of its products to become obsolete. The Company writes down excess and obsolete inventories based upon a regular analysis of inventory on hand compared to historical and projected demand. The determination of projected demand requires the use of estimates and assumptions related to projected sales for each product. These write downs can influence results from operations.

Account receivable, net and other receivables

Trade receivables are written off when there is no reasonable expectation of recovery. Indicators that there is no reasonable expectation of recovery include, amongst others, the failure of a debtor to engage in a repayment plan with the Company, and a failure to make contractual payments for a period of greater than 90 days past due.

Property, Plant and Equipment (PPE) & Construction in Progress (CIP)

In accordance with the ASC 360, Property, Plant, and Equipment, the Company’s PPE is stated at cost net of accumulated depreciation and impairment losses, if any. Costs incurred to acquire, construct, or install PPE, before the assets are ready for use, are capitalized in CIP at historical cost. The carrying amount of assets purchased or constructed out of the grant funds are presented net by deducting the grant proceeds received from the gross costs of the assets or CIP. CIP is not depreciated until such time when the asset is substantially completed and ready for its intended use. Expenditures for maintenance and repairs are charged to operations in the period in which the expense is incurred. Depreciation is calculated on a straight-line basis over the estimated useful life of the asset using the following terms:

Other equipment – 3 years
Production equipment – 2-4 years
Leasehold improvements – shorter of asset’s estimated useful life and the remaining term of the lease

12

The assets’ residual values, useful lives and methods of depreciation are reviewed periodically and adjusted prospectively, if appropriate. Equipment is derecognized upon disposal or when no future economic benefits are expected from its use. Any gain or loss arising upon de-recognition of the asset (calculated as the difference between the net disposal proceeds, if any, and the carrying value of the asset) is included in gain or loss on sale of assets in the consolidated statements of operations in the period the asset is derecognized.

Impairment of Long-lived Assets and Goodwill

Long-lived assets consist of property and equipment, right-of-use assets and other intangible assets. We assess impairment of assets groups, including intangible assets at least annually or more frequently if there are any indicators for impairment.

Goodwill represents the excess of the purchase price over the estimated fair value of the net assets acquired in a business combination. We perform an annual impairment test on goodwill in the fourth quarter of each fiscal year or when events occur or circumstances change that would, more likely than not, reduce the fair value of a reporting unit below its carrying value. We may first assess qualitative factors, such as general economic conditions, market capitalization, the Company’s outlook, market performance and forecasted financial performance to determine whether it is more likely than not that the fair value of a reporting unit is less than its carrying amount. If we determine it is more likely than not that the fair value of the reporting unit is greater than its carrying amount, an impairment test is not necessary. If an impairment test is necessary, we estimate the fair value of a related reporting unit. If the carrying value of a reporting unit exceeds its fair value, the goodwill of that reporting unit is determined to be impaired, and we will record an impairment charge equal to the excess of the carrying value over the related fair value of the reporting unit. If we determine it is more likely than not that goodwill is not impaired, a quantitative test is not necessary.

 

During the first quarterfiscal year ended June 30, 2023, the Company’s market capitalization significantly declined and recurring cash burn of the reporting unit and continuous cash support from the parent entity led management to reassess whether an impairment had occurred considering these qualitative factors. Management’s evaluation indicated that the goodwill related to its IFPG reporting unit was potentially impaired. The Company then performed a quantitative impairment test by calculating the fair value of the reporting unit and comparing that amount to it’s carrying value. Significant assumptions inherent in the valuation methodologies include, but were not limited to prospective financial information, growth rates, terminal value and discount rate. The Company determined the fair value of the reporting unit utilizing the discounted cash flow model. The fair value of the reporting unit was determined to be less than its carrying value. During the fiscal year ended June 30, 2020,2023, the Company purchased the license right procurement assets from LSBD forrecognized an amountimpairment charge of $976,3084.2 million in relationthe IFPG segment, which is related to the development and approval process forgoodwill associated with the Glucose Biosensor Technology inIFP Acquisition. Following the APAC region. The Company recordedimpairment charge the license at the historical carrying value in the books of LSBD whichgoodwill balance was $nil and recorded the amount paid as a deemed dividend. The Company has agreed to pay royalties of sales & milestones payments as defined.zero.

13

 

On September 12, 2019, the Company entered into an amended and restated license agreement for Saliva Biosensor Technology. On June 23, 2020, the Company entered into a license agreement with LSBD for the worldwide rights to SARS-CoV-2 application of the Saliva Glucose Biosensor.Intangible assets

 

In relation to these licenses, there is no set expiration date for the license. However, the exclusivityIntangible assets are considered long-lived assets and are recorded at cost, less accumulated amortization and impairment losses, if any. The definite lived intangible assets are amortized over their estimated useful lives, which do not exceed any contractual periods. Certain of the license granted under the license agreement runs until the expiration of the patent portfolio covered by the agreement which is currently until 2033. No royaltiesour intangible assets have been incurred throughassigned an indefinite life as we currently anticipate that these trade names and trademarks will contribute cash flows to September 30, 2022.the Company indefinitely. Indefinite-lived intangible assets are not amortized, but are evaluated at least annually to determine whether the indefinite useful life is appropriate. Amortization is recorded on a straight-line basis over their estimated useful lives. Intangible assets acquired from a foreign operation are translated from the foreign entity’s functional currency to the presentational currency based on the exchange rate at the reporting date.

 

On March 31, 2021, the Company entered into an agreement with LSBD to provide the Company an option to acquire an exclusive license to use LSBD’s intellectual property in the Saliva Glucose Biosensor in North America (the “Option Agreement”). The Option Agreement has a term of two yearsLeases ending March 31, 2023 and the exercise price for the option is $5,000,000. The fee of $500,000 incurred for the option was expensed in the period incurred.

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Trade, note and other receivables

 

Trade, note and other receivables are recorded net of allowances for uncollectible accounts. The Company evaluatesdetermines if an arrangement is a lease at its inception. Lease arrangements are comprised primarily of real estate for which the collectability of its accounts receivableright-of-use (“ROU”) assets and the corresponding lease liabilities are presented separately on the consolidated balance sheet.

ROU assets represent the right to use an underlying asset for the lease term and lease liabilities represent the obligation to make lease payments arising from the lease. ROU assets and lease liabilities are recognized at the lease commencement date based on various factors including historical experience, the lengthestimated present value of timelease payments over the receivableslease term. The lease term includes options to extend the lease when it is reasonably certain that the option will be exercised. Leases with a term of 12 months or less are past due andnot recorded on the financial healthunaudited condensed consolidated balance sheet.

The Company uses its estimated incremental borrowing rate in determining the present value of lease payments considering the term of the customer.lease, which is derived from information available at the lease commencement date, considering publicly available data for instruments with similar characteristics. The Company reserves specific receivables if collectabilityaccounts for the lease and non-lease components as a single lease component.

Employee benefits

The costs of short-term employee benefits are recognized as a liability and an expense, unless those costs are required to be recognized as part of the cost of inventories or non-current assets. The cost of any unused holiday entitlement is no longer reasonably assured. Based uponrecognized in the assessmentperiod in which the employee’s services are received. Termination benefits are recognized immediately as an expense when the company is demonstrably committed to terminate the employment of these factors, the Company did not record an allowance for uncollectible accounts as of September 30, 2022,employee or 2021.to provide termination benefits.

 

Net loss per share attributable to common shareholders (“EPS”)

 

The Company calculates earnings per share attributable to common shareholders in accordance with ASC 260, Earning Per Share. Basic net loss per share attributable to common shareholders is calculated by dividing net loss attributable to common shareholders by the weighted average number of common shares outstanding during the period. Diluted net loss per common share is calculated by dividing net loss attributable to common shareholders by weighted average common shares outstanding during the period plus potentially dilutive common shares, such as share warrants.

 

Potentially dilutive common shares shall beare calculated in accordance with the treasury share method, which assumes that proceeds from the exercise of all warrants are used to repurchase common share at market value. The number of shares remaining after the proceeds are exhausted represents the potentially dilutive effect of the securities.

 

As the Company has incurred net losses in all periods, certain potentially dilutive securities, including convertible preferred stock, warrants to acquire common stock, and convertible notes payable have been excluded in the computation of diluted loss per share as the effects are antidilutive.

 

14

Property, Plant and Equipment (PPE) & Construction in Progress (CIP)

Recent Accounting Pronouncements

In accordance with

The company assessed the ASC 360, Property, Plant, and Equipment, the Company’s PPE, except land, is stated at cost netadoption impacts of accumulated depreciation and impairment losses, if any. Land is stated at cost less any impairment losses. Costs incurred to acquire, construct, or install PPE, before the assets is ready for use, are capitalized in CIP at historical cost. The carrying amount of assets purchased or constructed out of the grant funds are presented net by deducting the grant proceeds received from the gross costs of the assets or CIP. CIP is not depreciated until such time when the asset is substantially completed and ready for its intended use.

Recentlyrecently issued accounting pronouncements

As the Company is an emerging growth company, we have elected to defer the adoption of new accounting pronouncements until they would apply to private companies.

Adopted:

In August 2020,standards by the Financial Accounting Standards Board (“FASB”) issued Accounting Standards Update (“ASU”) No. 2020-06, Debt – Debt with Conversion and Other Options (“ASU 2020-06”), which simplifies the guidance on the issuer’s accounting for convertible debt instruments by removing the separation models for (1) convertible debt with a cash conversion feature and (2) convertible instruments with a beneficial conversion feature. As a result, entities will not separately present in equity an embedded conversion feature in such debt and will account for a convertible debt instrument wholly as debt, unless certain other conditions are met. The elimination of these models will reduce reported interest expense and increase reported net income for entities that have issued a convertible instrument that is within the scope of ASU 2020-06. Also, ASU 2020-06 requires the application of the if-converted method for calculating diluted earnings per share and treasury stock method will be no longer available. The Company adopted ASU 2020-06 as of July 1, 2022. Adoption did not have a material impact on the Company’s financial statements.

11

Pending adoption:

In November 2021,statements as well as material updates to previous assessments, if any, from the Financial Accounting Standards Board (“FASB”) issued Accounting Standards Update (“ASU”) No. 2021-10, Government Assistance (“ASU 2021-10”). This update requires annual disclosures about transaction with a government that are accounted for by applying a grant or contribution accounting model by analogy. Required disclosures include (1) information about the nature of the transactions and the related accounting policy used to account for the transactions, (2) the line items on the balance sheet and income statement that are affected by the transactions, and the amounts applicable to each financial statement line item, and (3) significant terms and conditions of the transactions, including commitments and contingencies. ASU 2021-10 is applicable for fiscal years beginning after December 15, 2021, with early adoption permitted. The Company is planning to complete the required ASU 2021-10 disclosures with the filing of itsCompany’s Annual Report on Form 10-K for the fiscal year ending onended June 30, 2023. Based onThere were no new material accounting standards issued in 2024 that impacted the management’s assessment of ASU2021-10, this standard is not expected to have a material impact on the Company’s financial statements.Company.

 

In October 2021, the FASB issued ASU No. 2021-08, Business Combinations (Topic 805) – Accounting for Contract Assets and Contract Liabilities from Contracts with Customers (“ASU 2021-08”). ASU 2021-08 requires that an acquirer recognize and measure contract assets and contract liabilities acquired in a business combination in accordance with Topic 606, as if it had originated the contracts. Prior to this ASU, an acquirer generally recognized contract assets acquired and contract liabilities assumed that arose from contracts with customers at fair value on the acquisition date. The ASU is effective for fiscal years beginning after December 15, 2023, with early adoption permitted. The ASU is to be applied prospectively to business combinations occurring on or after the effective date of the amendment. The Company has not early adopted and continues to evaluate the impact of the provisions of ASU 2021-08 on its consolidated financial statements.

In June 2016, the FASB issued ASU No. 2016-13 (Topic 326), Financial Instruments – Credit Losses (“ASU 2016-13”). This update (i) significantly changes the impairment model for most financial assets that are measured at amortized cost and certain other instruments from an incurred loss model to an expected loss model which will be based on an estimate of current expected credit loss (“CECL”) (ASC 326-20); and (ii) provides for recording credit losses on available-for-sale (“AFS”) debt securities through an allowance account (ASC 326-30). The standard also requires certain incremental disclosures. Subsequently, the FASB issued several ASUs to clarify, improve, or defer the adoption of ASU 2016-13. ASU 2016-13, as amended by ASU 2019-10, is applicable for Smaller Reporting Companies (“SRCs”) for fiscal years beginning after December 15, 2022, with early adoption permitted. The Company has not early adopted the standard and continues to evaluate the impact.

In February 2016, the FASB issued ASU No. 2016-02, Leases (“ASU 2016-02”). This update requires all leases with a term greater than 12 months to be recognized on the balance sheet through a right-of-use asset and a lease liability and the disclosure of key information pertaining to leasing arrangements. This new guidance is effective for fiscal years beginning after December 15, 2021, and interim period within fiscal years beginning after December 15, 2022, as amended by ASU 2020-05 with early adoption permitted. The Company has not early adopted the standard and continues to evaluate the impact.

Concentration of credit risk

 

The Company places its cash and cash equivalents, which may at times be in excess of the Australia Financial Claims Scheme or the United States’ Federal Deposit Insurance Corporation insurance limits, with high credit quality financial institutions and attempts to limit the amount of credit exposure with any one institution.

 

Fair value of financial instruments

 

The accounting guidance defines fair value, establishes a consistent framework for measuring fair value and expands disclosure for each major asset and liability category measured at fair value on either a recurring or non-recurring basis. Fair value is defined as an exit price, representing the amount that would be received to sell an asset or paid to transfer a liability in an orderly transaction between market participants. As such, fair value is a market-based measurement that should be determined based on assumptions that market participants would use in pricing an asset or liability. As a basis for considering such assumptions, the accounting guidance establishes a three-tier fair value hierarchy, which prioritizes the inputs used in measuring fair value as follows:

 

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 that are not active, or other inputs that are observable or can be corroborated by observable market data for substantially the full term of the assets or liabilities.

Level 3-Unobservable inputs that are supported by little or no market activity and that are significant to the fair value of the assets or liabilities.

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Assets and liabilities measured at fair value are classified in their entirety based on the lowest level of input that is significant to the fair value measurement. The Company’s assessment of the significance of a particular input to the fair value measurement in its entirety requires management to make judgments and consider factors specific to the asset or liability.

The carrying amounts of cash equivalents, prepaid and other assets, accounts payable and accrued liabilities are representative of their respective fair values because of the short-term nature of those instruments.

 

15

NOTE 4. OTHER CURRENT ASSETSSEGMENT INFORMATION

Other current assets consist ofFASB ASC Topic 280, Segment Reporting, establishes standards for the following:manner in which companies report financial information about operating segments, products, services, geographic areas and major customers.

SCHEDULE OF OTHER CURRENT ASSETS

  September 30, 2022  June 30, 2022 
Intelligent Fingerprinting Limited note receivable $  $500,445 
Prepayments  41,532   116,525 
Goods and services tax receivable  55,852   57,746 
Deposits  44,493   46,602 
Other receivables  7,050   25,443 
Total $148,927  $746,761 

 

NOTE 5. OTHER NON-CURRENT ASSETSOur Segments

Other non-current assets consist of the following:

SCHEDULE OF OTHER NON-CURRENT ASSETS

  September 30, 2022  June 30, 2022 
Intelligent Fingerprinting Limited note receivable $504,938  $ 
Total $504,938  $ 

 

On June 16, 2022, the Company entered into an agreement with Intelligent Fingerprinting Limited (“IFP”), providing the Company with the exclusive right, until December 31, 2022, to evaluate and negotiate a transaction to acquire IFP or its assets. In consideration for this exclusivity, on June 16, 2022, the Company provided IFP with an unsecured term loan facility in the amount of $500,000, which was payable by IFP on the earliest of the consummationOperating segments are defined as components of an acquisition, 30 days followingentity for which separate financial information is available and that is regularly reviewed by the termination of exclusivity under the exclusivity agreement,Chief Operating Decision Maker (“CODM”) in deciding how to allocate resources to an event of default under the term loan facility agreement, or December 31, 2022. This $500,000 term note receivable bears an interest rate of 2% per annum above the Sterling Barclays Bank Base Rate from time to time.individual segment and in assessing performance. The Company subsequently completedCompany’s CODM is its Chief Executive Officer.

Following the acquisition of IFP, we conduct our business through two operating segments:

1)Commercially available Intelligent Fingerprinting Products (“IFPG” or “IFPG segment”)
2)Development Stage Saliva Glucose Biosensor Platform (“SGBP” or “SGBP segment”)

The Company has determined it operates in two operating and in connection therewith amendedreportable segments, as the termsCODM reviews financial information presented on a consolidated basis accompanied by disaggregated information about revenue and other income by product types for the purpose of allocating resources and evaluating financial performance. Currently, the Company has two products offerings.

The IFPG segment accounted for 100% of the term loan facility,Company’s revenue during the three months ended September 30, 2023. No revenue was recognized during the three months ended September 30, 2022.

16

The following table sets forth the Company’s revenue and other income by operating and reportable segment, disaggregated into geographic locations based on sales billed from the respective county, for the three months ended September 30, 2023. No revenue was recognized during the three months ended September 30, 2022.

SCHEDULE OF REVENUE AND OTHER INCOME SEGMENT

A)Revenue:

  IFPG  SGBP  Total 
  Three Months Ended September 30, 2023 
  IFPG  SGBP  Total 
United Kingdom $755,150  $  $755,150 
Australia  8,082      8,082 
Other  32,862      32,862 
Total Revenue $796,094  $  $796,094 

B)Other

  IFPG  SGBP  Total 
  Three Months Ended September 30, 2023 
  IFPG  SGBP  Total 
Australia $  $64,550  $64,550 
United Kingdom  45,321      45,321 
Total Government Support Income $45,321  $64,550  $109,871 

  IFPG  SGBP  Total 
  Three Months Ended September 30, 2022 
  IFPG  SGBP  Total 
Australia $  $311,320  $311,320 
United Kingdom         
Total Government Support Income $  $311,320  $311,320 

The Company operates in October 2022. See note 14.various geographic locations. The Company does not discretely allocate assets to its operating segments, nor does management evaluate operating segments using discrete asset information. The Company’s consolidated assets are not specifically ascribed to its individual reportable segments. Rather, assets used in operations are generally shared across the Company’s operating and reportable segments.

Property and equipment, net and operating lease right-of-use assets, by geographic location, are summarized as follows:

  

September 30,

2023

  June 30, 2023
(Audited)
 
Australia $731,579  $761,220 
United Kingdom  404,875   475,430 
Total $1,136,454  $1,236,650 

17

 

NOTE 5. INTELLIGENT FINGERPRINTING LIMITED ACQUISITION

On October 4, 2022, INBS acquired 100% of the outstanding shares of Intelligent Fingerprinting Limited (IFP), a company registered in England and Wales, pursuant to a Share Exchange Agreement, dated October 4, 2022 (the “Share Exchange Agreement”) by and among IFP, the holders of all of the issued shares in the capital of IFP (the “IFP Sellers”) and a representative of the IFP Sellers. IFP owns a portfolio of intellectual property for diagnostic tests and associated technologies, including drug testing through the analysis of fingerprint sweat. The acquisition of IFP has expanded the Company’s platform of rapid, non-invasive diagnostic testing technologies.

The table below summarizes the fair value of the consideration transferred in the acquisition (pre-Reverse Stock Split basis):

SCHEDULE OF FAIR VALUE OF THE CONSIDERATION TRANSFERRED IN THE ACQUISITION

Purchase consideration Amount 
Cash $363,500 
Note receivable settled for business acquisition  504,938 
Common Stock - 2,963,091 shares @ $0.5502 / share  1,630,293 
Series C Preferred Stock (base) - 2,363,003 shares @ 3 x $0.5502 / share  3,900,373 
Series C Preferred Stock (holdback) - 500,000 shares @ 3 x $0.5502 / share  825,300 
Purchase Consideration of Common Stock and Series C Preferred Stock  825,300 
Total purchase price $7,224,404 

Pursuant to the Share Exchange Agreement, the Company acquired from the IFP Sellers all of the issued and outstanding shares in the capital stock of IFP, and as consideration therefor, the Company issued and sold to the IFP Sellers upon the closing of the IFP Acquisition (the “IFP Closing”) an aggregate number of 148,183 (as adjusted for reverse stock split) shares of the Company’s common stock, and (ii) 2,363,003 shares of the Company’s Series C Convertible Preferred Stock, par value $0.01 per share (the “Series C Preferred Stock”).

Up to an additional 1,649,273 shares of Series C Preferred Stock have been reserved for potential future issuance by the Company, consisting of (i) 500,000 shares of Series C Preferred Stock, that are being held back from the IFP Sellers for one year after the IFP Closing to secure potential indemnification claims by the Company against the IFP Sellers and (ii) 1,149,273 shares of Series C Preferred Stock to certain lenders to IFP (the “IFP Lenders”). Each share of Series C Preferred Stock is convertible into 0.15 shares of Common Stock (subject to adjustment upon the occurrence of specified events), contingent upon approval by the Company’s stockholders.

Effective contemporaneously with the closing of the Company’s acquisition of IFP Closing, the Company entered into an amendment to the bridge facility agreement between the Company and IFP, dated as of June 16, 2022, pursuant to which, among other things, the $500,000504,938 (including accrued interest) loan from the Company to IFP pursuant theretothat will remain outstanding following the date of the IFP Closing until the second anniversary of the date of the IFP Closing (the “Company-IFP Loan Agreement”).

The loan receivable from IFP of $504,938 as of October 4, 2024.2022, was treated as a cash consideration in accordance with ASC 805, Business Combinations (“ASC 805”).

The Company entered into various loan agreements in the aggregate amount of $1,425,3071,254,270), including accrued interest, pursuant to which IFP is the borrower and the Company became a guarantor of IFP’s obligations thereunder (the “IFP Loan Agreements” and, together with the Company-IFP Loan Agreement, the “Loan Agreements”). Under the Loan Agreements, the loans thereunder remained outstanding following the IFP Closing and (x) the loans and certain accrued interest will convert into shares of IFP, which shares of IFP will be immediately transferred to the Company in exchange for shares of Series C Preferred Stock that are convertible into common stock (as set forth in the Share Exchange Agreement) following approval of the Company Stockholder Approval Matters (defined below) or (y) the loans and certain accrued interest will become repayable on the second anniversary of the date of the IFP Closing. The loans bear interest at 17% per annum on a compounded basis, increasing to 22% per annum on a compounded basis with effect from the date that falls 12 months following the date of the IFP Closing, if the Company Stockholder Approval Matters have not been approved by the Company’s stockholders by such date. The “Company Stockholder Approval Matters” means the approval by the Company’s stockholders of (i) the conversion of the Series C Preferred Stock into common stock and (ii) any amendments to, or adoption of, any option or warrant plans to give effect to the transactions contemplated under the Share Exchange Agreement.

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Each share of Series C Preferred Stock (other than the IFP Lender Preferred Shares) would automatically convert into common stock upon approval of the Company’s stockholders of the conversion of Series C Preferred Stock into common stock, and each IFP Lender Preferred Share would convert into common stock at the option of the applicable holder of such IFP Lender Preferred Shares following approval of the Company’s stockholders of the conversion of Series C Preferred Stock into common stock. In the event Company stockholder approval is not received, the convertible notes and accrued interest would remain outstanding. The number of shares of common stock into which the Series C Preferred Stock is convertible is subject to adjustment in the case of any stock dividend, stock split, combinations, or other similar recapitalization with respect to the common stock.

The rights, preferences and privileges of the Series C Preferred Stock are set forth in the Certificate of Designation of Preferences, Rights and Limitations of Series C Convertible Preferred Stock that the Company filed with the Secretary of State of the State of Delaware on October 4, 2022, as further described below (the “Series C Certificate of Designation”).

The Series C Preferred Stock does not have any voting rights (other than as required by law) and does not carry dividends or a liquidation preference. Each share of Series C Preferred Stock was initially convertible into 3 shares of common stock, subject to adjustment as noted above. Following the effectiveness of the 1-for-20 Reverse Stock Split effective on February 9, 2023, each share of Series C Preferred Stock is convertible into 0.15 shares of common stock. The loan receivable from IFP of $504,938 as of October 4, 2022, was treated as a cash consideration in accordance with ASC 805. See Note 11 for further information and disclosures relating to the conversion of the Series C Preferred Stock.

The Company incurred $806,397 of equity issuance costs in relation to issuing common and Series C Preferred Stock to acquire IFP. These costs were recognized as a reduction to additional paid-in capital on the condensed consolidated balance sheets.

On May 8, 2023, at a special meeting of the Company’s stockholders (the “Special Meeting”), the last of the remaining Company Stockholder Approval Matters were approved when the Company’s stockholders approved the full conversion of all Series C Preferred Stock and an increase in the number of shares authorized for issuance under the 2019 Long Term Incentive Plan (“2019 Plan” or the “Plan”). Subsequently, effective as of May 10, 2023, all 3,512,277 shares of outstanding Series C Preferred Stock (which included the 1,149,273 Lender Preferred Shares, but not the 500,000 Closing Holdback Shares (which are not deemed outstanding)) were converted into an aggregate of 526,818 shares of common stock.

The 500,000 Closing Holdback Shares (consisting of Series C Preferred Stock) are being held back from issuance to the IFP Sellers for one year after the IFP Closing in order to secure potential indemnification claims by the Company against the IFP Sellers. These Closing Holdback Shares, which are not deemed outstanding, are currently convertible into approximately 75,000 shares of common stock (subject to rounding for fractional shares).

The final allocation of the purchase price of IFP to the assets acquired and liabilities assumed, based on their relative fair values, is as follows:

SCHEDULE OF ASSETS ACQUIRED AND LIABILITIES ASSUMED, BASED ON THEIR RELATIVE FAIR VALUES

Allocation of purchase consideration Amount 
Assets:    
Cash and cash equivalents $174,481 
Inventory  774,625 
Other current assets  345,038 
Property and Equipment  52,170 
Intangible assets  5,463,000 
Goodwill  3,803,293 
Total assets acquired  10,612,607 
Liabilities:    
Accounts payable and accrued expenses  (1,027,302)
Notes payable  (677,137)
Convertible notes payable  (1,683,764)
Total liabilities assumed  (3,388,203)
Net assets $7,224,404 

Acquired intangible assets of $5,463,000 include technology of $5,119,000 (which is estimated to have a useful life of 7 years), customer relationships of $252,000 (which are estimated to have a useful life of 3 years), and trade names and trademarks of $92,000 (which are estimated to have an indefinite useful life). The value assigned to technology was determined using the multi-period excess earnings methodology under the income approach, the customer relationships was valued using the distributor method under the income approach, and the trade name and trademarks was valued using the relief from royalty method.

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The acquisition produced $3,803,293 of goodwill, which has been assigned to the IFPG reporting unit. The goodwill is attributable to a combination of IFP’s assembled workforce and other product and operating synergies. Goodwill arising from the IFP Acquisition is not deductible for tax purposes. During the fiscal year ended June 30, 2023, the full amount of goodwill was impaired. Refer to Note 3, summary of significant accounting policies, and Note 7, intangible assets for further information.

Transaction costs, except for the equity issuance costs discussed above, were not material and are included in selling, general and administrative expenses on the Company’s condensed consolidated statement of operations.

Intangible assets acquired from IFP were remeasured at September 30, 2023 and June 30, 2023 using the applicable spot rate.

Pro-Forma Results of Operations

Unaudited pro-forma consolidated results of operations for the three months ended September 30, 2023 are not required because the results of the acquired business are included in the Company’s results. The following unaudited pro-forma consolidated results of operations for the three months ended September 30, 2022, has been prepared as if the acquisition of IFP had occurred on July 1, 2022 and includes adjustments for amortization related to the valuation of acquired intangibles:

SCHEDULE OF UNAUDITED PRO-FORMA CONSOLIDATED RESULTS OF OPERATIONS

  As Reported  Pro Forma 
  Three Months Ended September 30, 2022 
  As Reported  Pro Forma 
Revenue $  $347,486 
Net loss  (1,214,078)  (2,455,633)
Net loss attributable to Intelligent Bio Solutions Inc.  (1,208,293)  (2,449,848)
Net loss per share, basic and diluted  (1.62)  (2.74)

NOTE 6. INVENTORIES

Inventories consist of the following:

SCHEDULE OF INVENTORIES

  

September 30,

2023

  June 30, 2023
(Audited)
 
Raw material and work-in-progress $  $419,889 
Finished goods  1,221,689   757,518 
Less: provision for inventory obsolescence  (256,598)  (197,500)
Inventory, net $965,091  $979,907 

20

NOTE 7. INTANGIBLE ASSETS, NET

Intangible assets, net consist of the following as of September 30, 2023:

SCHEDULE OF OTHER INTANGIBLE ASSETS

  Weighted average useful lives (years)  Acquisition cost  Effect of foreign currency  Accumulated amortization  Carrying value 
Technology 7 years  $5,119,000  $407,724  $935,292  $4,591,432 
Customer relationships 3 years   252,000   20,072   90,691   181,381 
Trade names and trademarks Indefinite   92,000   7,328      99,328 
Total intangible assets    $5,463,000  $435,124  $1,025,983  $4,872,141 

Intangible assets, net consist of the following as of June 30, 2023:

  Weighted average useful lives (years)  Acquisition cost  Effect of foreign currency  Accumulated amortization  Carrying value 
Technology 7 years  $5,119,000  $603,422  $780,500  $4,941,922 
Customer relationships 3 years   252,000   29,127   70,282   210,845 
Trade names and trademarks Indefinite   92,000   10,634      102,634 
Total intangible assets    $5,463,000  $643,183  $850,782  $5,255,401 

Intangibles assets recognized from the acquisition of IFP were allocated to the IFPG operating and reportable segment.

Expense related to the amortization of intangible assets for the three months ended September 30, 2023, was $175,201. There was no amortization of intangible assets during the three months ended September 30, 2022. Refer to Note 3, summary of significant accounting policies for further information.

Amortization expense for the intangible assets is expected to be as follows over the next five years, and thereafter:

SCHEDULE OF EXPECTED AMORTIZATION EXPENSES FOR INTANGIBLE ASSETS

     
Remainder of 2024 $641,947 
2025  855,929 
2026  787,911 
2027  765,239 
2028  765,239 
Thereafter  956,548 
Total $4,772,813 

There were no impairment charges related to intangible assets incurred in the periods presented.

21

NOTE 8. NOTE PAYABLE

As a result of the acquisition of IFP, the Company assumed a note payable due to a distributor of IFP. The unpaid principal balance of the loan will accrue interest at a rate of 0.97% per annum. The balance is offset by:

Payments of 10% of the Company’s monthly worldwide gross revenue received in the preceding month;
50% of sales by the company to the distributor.

The classification of the notes payables is based on sales forecast prepared by the management.

 

NOTE 6.9. ACCOUNTS PAYABLE AND ACCRUED EXPENSESLEASES

Accounts payable and accrued expenses consistIn relation to the IFP Acquisition, the Company assumed a non-cancelable operating lease agreement. The Company entered into another non-cancelable operating lease that commenced in May 2023. The leases have original lease periods expiring from August 2025 to April 2026. The lease agreements do not contain any material residual value guarantees or material restrictive covenants. The Company did not have any lease during the three months ended September 30, 2022.

The components of the following:lease expense are as follows:

SCHEDULE OF ACCOUNTS PAYABLE AND ACCRUEDFINANCE LEASE EXPENSES

  September 30, 2022  June 30, 2022 
Accounts and other payables $379,912  $715,902 
Accruals  658,633   909,187 
Total $1,038,545  $1,625,089 
  2023  2022 
  Three Months Ended September 30, 
  2023  2022 
Amortization of operating lease right-of-use assets $59,962  $ 
Interest on operating lease liabilities  21,171    
Total lease costs $81,133  $ 

 

As of September 30, 2023, the weighted average remaining lease-term and discount rate on the Company’s leases were 2.1 years and 13.2%, respectively.

As on

The reconciliation of the maturities of the operating leases to the operating lease liabilities recorded in the consolidated balance sheet as of September 30, 2022, the Company’s $658,633 of accruals include $415,350 related to legal and consulting fees, $135,615 related to development and regulatory approval expenses, $80,363 related to audit and accounting service fees, and $27,305 related to other general and administrative expenses.2023, is as follows:

SCHEDULE OF MATURITIES OF THE FINANCE LEASE TO THE FINANCE LEASE LIABILITIES

     
Remainder of 2024 $215,434 
2025  299,090 
2026  81,091 
Total lease payments  595,615 
Less: present value discount  (84,173)
Lease liabilities $511,442 

 

NOTE 7.10. SHAREHOLDERS’ EQUITY

As of September 30, 2022,2023, there were warrants outstanding to purchase 1,401,377426,521 and 52,400 Series A and Series B warrants wereshares of common stock, held by certain shareholders, respectively.shareholders. Each warrant is convertible into 1initially represented the right to purchase one share of the Company’s common stock.stock and was subject to adjustment upon the occurrence of specified events including reverse stock splits.

 

1322

NOTE 11. FAIR VALUE MEASUREMENTS

The Company has held back 500,000 Series C Preferred Stock, from the IFP Sellers for one year after the IFP Closing to secure potential indemnification claims by the Company against the IFP Sellers. Therefore, the final number of shares to be issued after the one-year measurement period is contingent on any potential claims and can be variable. Each share of Series C Preferred Stock is convertible into 0.15 shares of Common Stock (subject to adjustment upon the occurrence of specified events), contingent upon approval by the Company’s stockholders of the conversion of Series C Preferred Stock. These shares are reserved, not issued, or held in Escrow account. See Note 5 for further information and disclosures relating to the conversion of the Series C Preferred Stock.

The following table provides a reconciliation of the beginning and ending balance of the holdback Preferred Stock measured at fair value on a recurring basis during the period:

SCHEDULE OF PREFERRED STOCK AT FAIR VALUE ON RECURRING BASIS

  Preferred stock carried at fair value (Level 2) 
Balance at June 30, 2023 $208,500 
Fair value gain on revaluation of holdback Series C Preferred Stock  (131,250)
Balance at September 30, 2023 $77,250 

The Company did not have assets or liabilities carried at fair value using Level 1 inputs during the three months ended September 30, 2023 and 2022.

 

NOTE 8.12. RELATED PARTY TRANSACTIONS

LSBD

Sales to and purchases from related parties are made in arm’s length transactions both at normal market prices and on normal commercial terms. The following transactions occurred with LSBD during the comparative period July 1, 2021, to September 30, 2021:

The Company incurred a total of $nil during three months to September 2022 (September 2021: $119,652) towards overhead cost reimbursement which includes salaries, rents and other related overheads directly attributable to the Company which are included in general and administration expenses.

During the year ended June 30, 2021, the Company contributed a total of $2,600,000 towards budgeted development and commercialization costs to be incurred by BiosensX (North America) Inc. relating to the development and preparation for submission of the Saliva Glucose Biosensor connected with regulatory approval for the U.S. market by the U.S. Food & Drug Administration.

 

As of September 30, 2022,2023 and June 30, 2023, $8,5450 (September 30, 2021:and $68,8088,714), respectively, remains payable to LSBD in relation to overhead reimbursements detailed above.reimbursements.

NOTE 9. INVESTMENT IN AFFILIATE

On May 29, 2020, LSBD, issued 14,000,000 common shares of BiosensX (North America) Inc. to the Company at par value of $0.001 per share. This transaction provided the Company with a 50% interest in BiosensX (North America) Inc., the holder of the technology license for the North America region.

The investment in BiosensX (North America) Inc. is accounted for by use of the equity method in accordance with ASC 323, Investments - Equity Method and Joint Ventures.

At the date of this transaction, LSBD was the parent of both the Company and BiosensX (North America) Inc., the transfer of BiosensX shares to the Company was deemed to be a common control transaction. As a result of the share transfer, the Company has significant influence over BiosensX (North America) Inc.

During the year ended June 30, 2022, LSBD sold all its shares in INBS. The Company determined whether it has a controlling financial interest in BiosensX (North America) Inc. by first evaluating whether the entity is a voting interest entity or a VIE under GAAP. Voting interest entities are entities in which the total equity investment at risk is sufficient to enable the entity to finance itself independently and provides the equity holders with the obligation to absorb losses, the right to receive residual returns and the right to make decisions about the entity’s activities. The Company consolidates voting interest entities in which it has all, or at least a majority of, the voting interests. As defined in applicable accounting standards, VIEs are entities that lack one or more of the characteristics of a voting interest entity. A controlling financial interest in a VIE is present when an enterprise has both the power to direct the activities of the VIE that most significantly impact the VIE’s economic performance and an obligation to absorb losses or the right to receive benefits that could potentially be significant to the VIE. The enterprise with a controlling financial interest, known as the primary beneficiary, consolidates the VIE. The Company concluded that it does not have a controlling financial interest in BiosensX (North America) Inc., hence it continues to recognize its investments in BiosensX (North America) Inc. using the equity method.

The carrying amount of investments in BiosensX (North America) Inc. was $nil as of September 30, 2022, and June 30, 2022.

NOTE 10. CONSTRUCTION IN PROGRESS

During the three months ended September 30, 2022, the Company incurred costs of $49,242 towards the construction of R&D and manufacturing facility at the University of Newcastle. The Australian government reimbursed the Company 50% of the costs incurred towards building of the facility. The carrying amounts of the Constructions in Progress (CIP) is calculated by deducting the reimbursement from total cost incurred.

The following table summarizes the amount of CIP recorded in the Condensed Consolidated Balance Sheets:

SUMMARY OF AMOUNT RECORDED IN THE CONSOLIDATED BALANCE SHEETS

  September 30, 2022  June 30, 2022 
Investments in construction in progress $832,058  $782,816 
Less: 50% contributed under government grant  (416,029)  (391,408)
Carrying amount $416,029  $391,408 

14

NOTE 11.13. COMMITMENTS AND CONTINGENCIES

During February 2021November 2022, the Company signed a deed of confirmation and variation with the University of Newcastle for the research and development of the Saliva Glucose Biosensor and the SARS-CoV-2 Antibody Biosensor. The Company agreed to pay the University of Newcastle $2,054,880847,021, of which $135,615847,021 remains payable as of September 30, 2022.2023.

 

The Company has no material future minimum leasepurchase commitments. For commitments or purchase commitments.under non-cancellable leases, refer to Note 9.

 

From time to time, the Company may become a party to various legal proceedings arising in the ordinary course of business. Based on information currently available, the Company is not involved in any pending or threatened legal proceedings that it believes could reasonably be expected to have a material adverse effect on its financial condition, results of operations or liquidity. However, legal matters are inherently uncertain, and the Company cannot guarantee that the outcome of any potential legal matter will be favorable to the Company.

 

23

NOTE 12. INCOME TAX

The Company shall file its income tax returns with the Internal Revenue Service and Australian Taxation Office. The Company has operating losses carried forward of $28,443,205 which are derived from its operations in Australia and the US and are available to reduce future taxable income. Such loss carry forwards may be carried forward indefinitely, subject to compliance with tests of continuity and additional rules.

The net operating loss carried forward gives rise to a deferred tax asset of approximately $6,325,630. However, the Company has determined that a valuation allowance of $6,325,630 against such deferred tax asset is necessary, as it cannot be determined that the carry forwards will be utilized.

 

NOTE 13.14. LOSS PER SHARE

Basic loss per common share is computed by dividing net loss allocable to common shareholders by the weighted average number of shares of common stock or common stock equivalents outstanding. Diluted loss per common share is computed similar to basic loss per common share except that it reflects the potential dilution that could occur if dilutive securities or other obligations to issue common stock were exercised or converted into common stock.

SCHEDULE OF BASIC LOSS PER COMMON SHARE POTENTIAL DILUTIVE SECURITIES

  2022  2021 
  Three Months Ended September 30, 
  2022  2021 
Net loss attributable to Intelligent Bio Solutions Inc. $(1,208,293) $(1,432,652)
Basic and diluted net loss per share attributed to common shareholders $(0.08) $(0.10)
Weighted-average number of shares outstanding  14,889,904   14,006,127 

15

The following outstanding warrants, options and preferred shares were excluded from the computation of diluted net loss per share for the periods presented because their effect would have been anti-dilutive:

SCHEDULE OF ANTI-DILUTIVE WARRANTS

         2023  2022 
 Three Months Ended September 30,  September 30, 
 2022  2021  2023  2022 
Warrants - Common stock (March 23 public raise)  3,270   - 
Warrants - Series A  1,401,377   1,401,377   70,068   70,068 
Warrants - Series B  52,400   59,782   2,620   2,620 
Warrants issued to underwriters  63,529   63,529 
Private placement warrants (Dec 2022)  26,478   - 
Warrants issued to Winx Capital Pty Ltd  1,324   - 
Warrants issued to underwriters (IPO)  3,177   3,177 
Warrants issued to underwriters (March 23 public raise)  32,750   - 
Pre IPO warrants  2,736,675   2,736,675   136,834   136,834 
Warrants issued to the licensor  3,000,000   3,000,000 
Warrants issued to licensor - LSBD  150,000   150,000 
Anti-dilutive  150,000   150,000 

NOTE 14.15. SUBSEQUENT EVENTS

On August 5, 2022,Subsequent to the quarter ended September 30, 2023, on October 4, 2023, the Company filedcompleted a registration statement on Form S-8 with the SEC to registercapital raise consisting a total of 500,0002,232,221 shares of common stock, 5,728,723 shares of the Company’s common stock issuable pursuantSeries E Convertible Preferred Stock (“Preferred Stock”) that were issued in lieu of Common Stock, 7,960,944 warrants to purchase shares of Common Stock that will expire on the five-and-a-half-year anniversary of the original issuance date (the “Series E Warrants”), and 7,960,944 warrants to purchase shares of Common Stock that will expire on the one-and-a-half-year anniversary of the original issuance date (the “Series F Warrants”, collectively with the Series E Warrants, the “Warrants”). Each Unit consists of one share of Common Stock (or one share of Preferred Stock), one Series E Warrant and one Series F Warrant. The Units were priced at a combined public offering price of $0.55 per Unit for initial gross proceeds of approximately $4.378 million. Net proceeds to the Company’s 2019 Long Term Incentive Plan (the “2019 Plan”). On October 6, 2022,Company, after deducting the underwriting discounts and commissions and estimated offering expenses payable by the Company, issued were approximately $500,0003.35 common shares to its employees under the 2019 Plan. These shares vested immediately upon issuance, and the respective holders thereof had the immediate right to receive all shares of common stock issued under the 2019 Plan.million.

 

On October 4, 2022, the Company acquired Intelligent Fingerprinting Limited (“IFP”), a company registered in England and Wales, through a share exchange agreement with the shareholders of IFP (the “Sellers”). The Company purchased 100% of the issued shares of IFP by issuing 2,963,091 shares of the Company’s common stock and 2,363,003 shares of the Company’s series C convertible preferred stock (“preferred stock”)Subsequent to the Sellers. Up to an additional 1,649,273 shares of preferred stock have been reserved for potential future issuance by the Company, consisting of (i) 500,000 shares of preferred stock held back from the Sellers for one year after the closing of the acquisition to secure potential indemnification claims by the Company against the Sellers and (ii) 1,149,273 shares of preferred stock for Sellers who are also the IFP convertible loan holders and, at each loan holder’s respective option, convert such the outstanding convertible loans to IFP into shares of Company preferred stock, contingent upon approval of the Company’s stockholders of the conversion of the preferred stock into common stock. Each preferred share will be convertible into three shares of Company common stock, contingent upon approval by the Company’s stockholders. In addition, the Company is obligated to pay the cash bonuses of approximately $350,150 (consisting of £239,707 and $83,043) to certain current and former IFP employees and directors in two equal installments. The first payment was made immediately following the closing of the acquisition, and the second payment is required to be made on the six-month anniversary of closing date of the acquisition. The acquisition of IFP will expand the Company’s platform of rapid, non-invasive diagnostic testing technologies.

In conjunction with the IFP acquisition, the Company has agreed to make a Company’s stock option plan available to IFP employees for up to 1,000,000 shares common stock following the closing of the acquisition. An equal number of stock options will be granted to the Company’s employees, for an aggregate amount of 2,000,000 Company stock options.

Due to the limited time between the transaction date and the Company’s filing of this Quarterly Report on Form 10-Q for the quarter ended September 30, 2022, initial accounting for the business combination is incomplete and the Company is not yet able2023, through to disclose the provisional amountsNovember 7, 2023, a total of 4,571,761 Series E Convertible Preferred Stock were converted to be recognized as of the acquisition date for assets acquired and liabilities assumed, and the pro forma revenues for the combined entity. Management is evaluating the transaction costs and the fair value of consideration transferred, assets acquired, and liabilities assumed. The Company expects to provide the preliminary purchase price allocation information in the Quarterly Report on Form 10-Q for the quarter ending December 31, 2022.common stock.

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

 

You should read the following discussion in conjunction with our audited historical consolidated financial statements, which are included in the 20222023 Form 10-K and our unaudited condensed consolidated financial statements for the fiscal quarter ended September 30, 20222023, included elsewhere in this Quarterly Report on Form 10-Q. This Management’s Discussion and Analysis of Financial Condition and Results of Operations contains statements that are forward-looking. These statements are based on current expectations and assumptions that are subject to risks, uncertainties, and other factors. Actual results could differ materially because of the factors discussed below or elsewhere in this Quarterly Report on Form 10-Q. See Part II, Item 1A. “Risk Factors” of this Quarterly Report on Form 10-Q and Part I, Item 1A. “Risk Factors” of the 20222023 Form 10-K.

 

Forward-Looking Information

Forward-Looking Information

All statements other than statements of historical fact or relating to present facts or current conditions included in this Quarterly Report on Form 10-Q are forward-looking statements. Forward-looking statements include, but are not limited to, statements regarding expectations, hopes, beliefs, intentions or strategies regarding the future. In addition, any statements that refer to projections, forecasts or other characterizations of future events or circumstances, including any underlying assumptions, are forward-looking statements. These statements may include words such as “anticipate,” “estimate,” “expect,” “project,” “plan,” “intend,” “believe,” “may,” “should,” “can have,” “likely” and the negative of such words and other words and terms of similar meaning, but the absence of these words does not mean that a statement is not forward-looking.

The forward-looking statements contained in this Quarterly Report on Form 10-Q are based on our current expectations and beliefs concerning future developments and their potential effects on us. These forward-looking statements are subject to a number of risks, uncertainties and assumptions, including those described in “Item 1A — Risk Factors” of this Quarterly Report on Form 10-Q and in our 2022

All statements other than statements of historical fact or relating to present facts or current conditions included in this Quarterly Report on Form 10-Q are forward-looking statements. Forward-looking statements include, but are not limited to, statements regarding expectations, hopes, beliefs, intentions, or strategies regarding the future. In addition, any statements that refer to projections, forecasts or other characterizations of future events or circumstances, including any underlying assumptions, are forward-looking statements. These statements may include words such as “anticipate,” “estimate,” “expect,” “project,” “plan,” “intend,” “believe,” “may,” “should,” “can have,” “likely” and the negative of such words and other words and terms of similar meaning, but the absence of these words does not mean that a statement is not forward-looking.

The forward-looking statements contained in this Quarterly Report on Form 10-Q are based on our current expectations and beliefs concerning future developments and their potential effects on us. These forward-looking statements are subject to a number of risks, uncertainties and assumptions, including those described in “Item 1A — Risk Factors” of this Quarterly Report on Form 10-Q and in our 2023 Form 10-K. Moreover, we operate in a very competitive and rapidly changing environment. New risks emerge from time to time. It is not possible for our management to predict all risks, nor can we assess the impact of all factors on our business or the extent to which any factor, or combination of factors, may cause actual results to differ materially from those contained in any forward-looking statements we may make. In light of these risks, uncertainties and assumptions, the future events and trends discussed in this Quarterly Report on Form 10-Q may not occur and actual results could differ materially and adversely from those anticipated or implied in the forward-looking statements.

 

You should not rely upon forward-looking statements as predictions of future events. The events and circumstances reflected in the forward-looking statements may not be achieved or occur. Although we believe that the expectations reflected in the forward-looking statements are reasonable, we cannot guarantee future results, levels of activity, performance, or achievements. Except as required by the federal securities laws, we are under no duty to update any of these forward-looking statements after the date of this Quarterly Report on Form 10-Q or to conform these statements to actual results or revised expectations.

 

Overview

 

Intelligent Bio Solutions Inc. (formerly known as GBS Inc.) (“INBS”) and its wholly owned Delaware subsidiary, GBS Operations Inc. were each formed on December 5, 2016, under the laws of the state of Delaware. Our Australian subsidiary Intelligent Bio Solutions (APAC) Pty Ltd (formerly known as Glucose Biosensor Systems (Greater China) Pty LtdLtd) was formed on August 4, 2016, under the laws of New South Wales, Australia and was renamed to GBSIntelligent Bio Solutions (APAC) Pty Ltd on October 14, 2020. Glucose Biosensor Systems (Japan) Pty Ltd and Glucose Biosensor Systems (APAC) Pty Ltd were formed under the laws of New South Wales, Australia on February 22, 2017 and February 23, 2017 respectively.January 6, 2023. On October 26,4, 2022, the Company changed its corporate nameINBS acquired Intelligent Fingerprinting Limited (IFP), a company registered in England and Wales (the “Name Change”) from “GBS Inc.” to “Intelligent Bio Solutions Inc.” For purpose of the Quarterly Report on Form 10-Q, the terms “Company”, “we,” “us” and “our” refer to INBS and its consolidated subsidiaries unless context indicates otherwise.IFP Acquisition). Our headquarters are in New York, New York.

 

We are a medical technology company operating acrossfocused on developing and delivering intelligent, rapid, non-invasive testing and screening solutions. We operate globally with the Asia-Pacific region (the “APAC Region”) with an objective to introduceof providing innovative and deliver intelligent pain free diagnostic tests. We also have an interest inaccessible solutions that improve the North America region. Our goal is to expand the global footprintquality of our drug screening tests following our recent acquisition of Intelligent Fingerprinting Limited, while continuing to develop our Biosensor Platform that we license from Life Science Biosensor Diagnostics Pty Ltd (“LSBD” or the “Licensor”). This will be followed by developing both of our platforms to their full capacity across multiple diagnostic modalities of immunology, hormones, chemistry, tumor markers and nucleic acid tests.

Highlights of Achievements during the Quarter

Highlights of our major achievements for the quarter ended September 30, 2022 are:life.

During the quarter ended September 30, 2022 the Company negotiated the acquisition of Intelligent Fingerprinting Limited (“IFP”), a company registered in England and Wales and on October 4, 2022 the Company closed on the acquisition of IFP (the “Acquisition”).

In connection with the Acquisition, on October 4, 2022, the Company entered into a Share Exchange Agreement (the “Share Exchange Agreement”) with IFP, the holders of all of the issued shares in the capital of IFP (collectively, the “Sellers”) and the “Sellers’ Representatives” named therein (the “Sellers’ Representatives”).

 

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Pursuant to the Share Exchange Agreement, among other things, the Company acquired from the Sellers all of the issued shares in the capital of IFP, and as consideration therefor the Company issued and sold to the Sellers upon the closing of the Acquisition (the “Closing”) an aggregate number of (i) 2,963,091 shares of the Company’s common stock, and (ii) 2,363,003 shares of the Company’s series C convertible preferred stock, par value $0.01 per share (the “Preferred Stock”). Up to an additional 1,649,273 shares of Preferred Stock have been reserved for potential future issuance by the Company, consisting of (i) 500,000 shares of Preferred Stock, representing approximately 10% of the total Acquisition consideration, that are being held back from the Sellers for one year after the Closing to secure potential indemnification claims by the Company against the Sellers and (ii) 1,149,273 shares of Preferred Stock to certain lenders to IFP (the “Lenders”) who may, at each such Lender’s respective option, convert such Lender’s respective loans to IFP into shares of Preferred Stock, contingent upon approval of the Company’s stockholders of the conversion of Preferred Stock into Common Stock, as described below (the “Lender Preferred Shares”). Each Preferred Share would be convertible into three shares of Common Stock, contingent upon approval by the Company’s stockholders.

Also pursuant to the Share Exchange Agreement, the Company has an obligation to provide IFP with cash in an amount such that IFP is able to pay cash payments to certain current and former United Kingdom and United States-based employees and directors (the “IFP Bonus Recipients”), in aggregate amounts of £239,707 and $83,043, respectively (the “Cash Bonuses”), plus any applicable employer’s National Insurance contributions. The Cash Bonuses are being paid to the IFP Bonus Recipients in two equal instalments, with the first payment made immediately following the Closing and the second payment to be made on the six-month anniversary of such date.

Also pursuant to the Share Exchange Agreement, the Company has agreed to make available to the employees of IFP (the “IFP Employees”) a Company stock option plan in form and substance satisfactory to the Company in relation to up to 1,000,000 shares Common Stock following the Closing on the basis that an equal number of Company stock options will be granted to the IFP Employees and Company employees up to an aggregate amount of 2,000,000 Company stock options.

Each of the Company, IFP and the Sellers made certain customary representations and warranties and agreed to certain covenants in the Share Exchange Agreement.

On July 13, 2022, INBS completed Institutional Review Board (IRB) approved clinical studies at the Diabetes Research Institute of Sutter Health’s Mills-Peninsula Medical Center (MPMC) in San Mateo, California. The study design was intended to support the clinical development of its next-generation Saliva Glucose Biosensor. A total of 40 adult subjects with type 2 diabetes were recruited for the study. Nearly 1,400 samples of blood and oral fluids were collected and analyzed. The subsequent statistical analysis of the correlation of glucose levels among these sample types will act as foundation for building a robust portfolio of prospective clinical evidence, forming the backbone for future regulatory submissions. The Company anticipates further clinical studies in the fourth quarter of this calendar year and will utilize Saliva Glucose Biosensors fabricated at the Centre for Organic Electronics in New South Wales, Australia
We are continuing to develop our R&D and manufacturing facility at University of Newcastle, Australia. During the quarter, we commenced the design of the facility and constructions of the facility is expected to start in second quarter of calendar year 2023.
During the quarter, we received and commenced installation of new lab equipment including the Mass Spectrometer and GPC systems, which allows to improve the specificity, sensitivity, and reproducibility of our Biosensor technology.

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The Saliva Glucose Biosensor

The APAC Region includes over 164 million people living with diabetes, which accounts for approximately 38% of the world’s diabetic population. Rapid urbanization, unhealthy diets and increasingly sedentary lifestyles have resulted in ever increasing rates of obesity and diabetes across the region.

Self-testing blood glucose monitors were introduced to the market in the 1970s and, since then, the method of glucose self-monitoring has not meaningfully changed. The industry remains dominated by invasive methods that ultimately use blood or interstitial fluid to measure glucose. We believe the methodology of the Company’s Saliva Glucose Biosensor (“SGB” and, together with the software app that interfaces the SGB with the Company’s digital information system, the “SGT”) represents a breakthrough in glucose monitoring as it represents the only non-invasive, painless, and cost-effective saliva-based method of measuring glucose levels. The biosensor technology has been developed over several decades of university-based scientific research and has been extensively referenced in scientific literature.

The SGB is an organic, thin-film transistor, which in its structure embeds the glucose oxidase enzyme (referred to as “GOX”). When the single-use SGB interacts with saliva it initiates a sequence of enzymatic and electrochemical reactions, producing an electrical signal directly correlated to the amount of glucose present in the saliva. This measurement is then converted into a real-time saliva glucose reading, through the biosensor app installed on a smart device or a dedicated reader. The reading may then be stored in a cloud-based digital information system.

The patent protected SGB is able to detect glucose in saliva at concentrations between 8 and 200 µM and exhibits linear glucose sensing characteristics at these concentrations, sensing glucose at levels 100 times lower than blood.

In our development of the SGT, we aim to go beyond the innovation of changing the sampling medium from blood to saliva, and further create value for the patient and the payers by decreasing the cost of managing diabetes, improving the outcomes of the disease and providing convenience in testing methodology. This will be achieved by directly transferring the SGB reading from the smart device or dedicated reader to a cloud-based digital information system to enable all patients the option to create their own medical records where the SGB results will be uploaded.

 

Our digital information system is intended to be interfaced to an artificial intelligence system and will be able to, at the patient’s or authorized care giver’s direction, disseminate patient data to a remote caregiver, a service for consultation or to any other individual with whom the patient chooses to share his or her glucose level measurements. We believe patients and payers will be able to leverage our digital information system to decrease cost and improve outcomes and convenience.

With the SGB we aim to drive economic value beyond the revenue stemming from the sale of the SGB units – it also allows for monetization and the creation of separate revenue streams from the patient network and other data that resides within our digital information system, by way of the following:

Data usage. The usage of the data, and the analysis and interpretation of the data, to improve patients’ conditions and leveraging this insight to improve patient care.
Safe data sharing. The provision of data sharing services between users/patients, authorized care givers and authorized medical practitioners.
Data collection. The collection of anonymized data, its aggregation with other data from multiple sources and multiple health devices and its combination with non-health data.

We plan to leverage this usage, safe sharing and collection of data in the following four revenue-generating channels:

Direct Monetization Channel. This channel focuses on the development of revenue based on commercial relationships for the use of anonymized and compliant information derived from data generation. These services may include, but will not be limited to:

Fee for service, per performed action by pharma, or other commercial partners.
Subscription, regular recurring payments for continued access to service.
Prescription, value acknowledged by payer reimbursement per active user.
Third party coverage, other industry/retail players pay fee for their own customers.
Risk sharing/profit sharing, success-based payment models.
Advertising, third party ads tailored to demographic data leveraging characteristics unique to channel.
Added value of INBS brand loyalty.

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Commercial Adjacencies Channel. This channel focuses on the development of revenue from data generated through patient engagement and market insights from a clinical and medical perspective. These services may include, but will not limited to:

Medical – Generation of Patient Reported Outcomes, or “PROs”.
Data – Market insights, clinical trial recruitment for third parties, e.g., pharmaceutical companies or clinical research organizations.
Consumer – e-commerce platform, third party customer care, advertising.

Product and Service Bundles Channel. This channel focuses on ancillary revenue generated through bespoke service opportunities across the industry, for example, by working with insurers to develop products that integrate the usage of testing as part of their service offering. These services may include, but will not be limited to:

Over-the-counter model.
Bundle payment model with insurance subsidy.
Pay for outcomes model.

Core Operations Synergy Channel. Through combining the data generation with the use of artificial intelligence, we expect to have a deep insight into our customer base, providing an elevated level of customer insight. It is expected that this insight will drive high customer retention levels and generate a considerable number of broader revenue opportunities through direct and specific interaction with our customer base. These opportunities may include, but will not be limited to:

Direct access to customers for better experience in customer care.
Peer learning and support to decrease customer care resource commitment.
Direct market and customer insights (including better understanding of customer journey).
More customer data for targeted marketing & marketing impact monitoring.
New cost effective, digital marketing channel enabling agile marketing approach.
PRO data to support unique marketing claims.
Higher engagement, customer loyalty and customer lifetime value.
Consumer driven innovation and customer involvement in development.
Involvement in testing & refining to develop demand-oriented products rapidly.
Easy and fast clinical evaluation recruitment.
PRO to support regulatory approval / market access for platform tests under development.

The SGB has been under continuous development for over seven years, first by the University of Newcastle, Australia, then by the Licensor and us. The SGB development program is currently at the design and manufacturing process development stage, which includes the testing needed to verify and validate the final product. This stage involves implementation of the clinical evidence module, which incorporates the commercial production of the investigative biosensor devices to commence the clinical evaluation of analytical performance of the device and generate the clinical evidence necessary to gain regulatory approval.

On May 1, 2020, the Licensor filed a submission with the FDA for the Saliva Glucose Biosensor Diagnostic Test, currently in development as a point-of-care test intended to replace blood glucose testing for diabetes management. Following the 513(g) submission to the FDA (Submitted May 1, 2020), it was determined that the Company could seek the De Novo application pathway for the Saliva Glucose Biosensor Diagnostic Test, we were appointed an expert contact person, Acting Branch Chief from the Diabetes Diagnostic Devices Branch. We have further commenced planning discussions with the FDA Office of In Vitro Diagnostics and Radiological Health and the Office of Product Evaluation and Quality pertaining to the clinical development and study plan of the Saliva Glucose Biosensor. We expect to leverage synergies from the planned approval process with the FDA within the Asia Pacific region, We will first seek regulatory approval with the Therapeutic Goods Administration (TGA) in Australia. However, we intend to apply for regulatory approval in each jurisdiction across the APAC Region.

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The SGB is manufactured using modified reel-to-reel printing technology that was developed at the Australian National Fabrication Facility. This technology allows mass volume printing at a low cost. Previous research published in the journal Solar Energy Materials and Solar Cells has shown that the cost of manufacture of printed organic electronic devices (like the SGB) using mass volume printing is $7.85 per square meter, with an uncertainty of 30%. The size of the printed biosensors is approximately one square centimeter, resulting in a manufacturing cost per biosensor of approximately $0.01.

We anticipate that the non-invasive nature of saliva-based glucose testing will make patients more amenable to glucose monitoring, with the expected result of increasing the number of times a patient tests per day. The data generated by the SGB, combined with the interface of the smart device or dedicated reader with our digital information system and the artificial intelligence feedback, will allow the patient to achieve better glucose control through a practical understanding of lifestyle factors that affect glucose levels, thereby helping prevent or delay diabetes complications and ultimately personalizing diabetes management.

Initial public offering & share structure

On December 28, 2020, the Company closed its initial public offering (“IPO”) and sold 1,270,589 units, consisting of (a) one share of the Company’s common stock (or, at the purchaser’s election, one share of Series B Convertible Preferred Stock), (b) one Series A warrant (the “Series A Warrants”) to purchase one share of the Company’s common stock at an exercise price equal to $8.50 per share, exercisable until the fifth anniversary of the issuance date, and (c) one Series B warrant (the “Series B Warrants”) to purchase one share of the Company’s common stock at an exercise price equal to $17.00 per share, exercisable until the fifth anniversary of the issuance date and subject to certain adjustment and cashless exercise provisions. The public offering price of the shares sold in the IPO was $17.00 per unit. In aggregate, the units issued in the offering generated $17,732,448 in net proceeds, which amount is net of $1,714,001 in underwriters’ discount and commissions, and $2,153,564 in offering costs. The Company also issued to the underwriter an option, exercisable one or more times in whole or in part, to purchase up to 190,588 additional shares of common stock and/or Series A Warrants to purchase up to an aggregate of 190,588 shares of common stock and/or Series B Warrants to purchase up to an aggregate of 190,588 shares of common stock, in any combinations thereof, from us at the public offering price per security, less the underwriting discounts and commissions, for 45 days after the date of the IPO to cover over-allotments, if any (the “Over-Allotment Option”). 

Upon the closing of the IPO, all shares of preferred stock then outstanding were automatically converted into 2,810,190 shares of common stock, and all convertible notes then outstanding were automatically converted into 710,548 shares of common stock. 

Certain preferred shareholders were issued warrants that, following the Company’s completed IPO, allow the holder to acquire 2,736,675 shares of common stock at the IPO price during years two through three following the IPO. At the exercise date, the shareholder must hold for each warrant to be exercised, one underlying common share to exercise the option. The warrants are not transferable and apply to the number of shares that were subscribed for.

The share structure as of November 10, 2022 was as follows:current product portfolio includes:

 

 18,352,995Intelligent Fingerprinting Platform - Our proprietary portable platform analyzes fingerprint sweat using a one-time (recyclable) cartridge and portable handheld reader. Our flagship product from this platform, which is commercially available in certain countries outside of Issued Common Stockthe United States, is the Intelligent Fingerprinting Drug Screening System (the “IFP System” or “IFP Products”), a two-part system that consists of non-invasive, sweat-based fingerprint diagnostic testing products designed to detect drugs of abuse including opioids, cocaine, methamphetamines, benzodiazepines, cannabis, methadone, and buprenorphine. The system comprises a small, tamper-evident drug screening cartridge onto which ten fingerprint sweat samples are collected in under a minute, before the portable analysis unit provides an on-screen result in under ten minutes. Samples collected with our confirmatory kits can also be sent to a third-party laboratory service provider to perform confirmation testing. Customers include safety-critical industries such as construction, transportation and logistics firms, manufacturing, engineering, drug treatment organizations in the rehabilitation sector, and judicial organizations.
 1,401,377The Biosensor Platform – Our “Biosensor Platform” consists of Series A warrants exercisablea small, printable modified organic thin-film transistor strip that we license across the Asia Pacific Region from Life Science Biosensor Diagnostics Pty Ltd (“LSBD” or “Licensor”). The Biosensor Platform, which is designed to detect multiple biological analytes by substituting the Glucose Oxidase (“GOX”) enzyme with a suitable alternative for each analyte, is currently in the development stage. Our flagship product candidate based on the Biosensor Platform technology is the Saliva Glucose Biosensor (“SGB” and, together with a software app that interfaces the SGB with the Company’s digital information system, the Saliva Glucose Test or “SGT”), a Point of Care Test (POCT) expected to complement the invasive finger prick blood glucose monitoring test for diabetic patients. Our products based on the SGT are referred to herein as the “SGT products.”

These platform technologies have the potential to develop a range of POCT’s including the modalities of clinical chemistry, immunology, tumor markers, allergens, and endocrinology.

Highlights of Achievements

Our major achievements through the quarter ended September 30, 2023:

On September 27, 2023, the Company announced that its Intelligent Fingerprinting Drug Screening business had obtained recertification for the latest ISO 13485: 2016 harmonized quality management system standard for the medical device industry. The recertification is effective October 14, 2023, and will be valid for three years. ISO 13485:2016 is the international standard for medical devices quality management system certification and is a requirement for medical device manufacturers operating across key regions, including the USA, Canada, Europe, Japan, Singapore, Malaysia and Saudi Arabia. Last year the US Food and Drug Administration published a proposed rule to harmonize its medical device quality management system, 21 CFR Part 820, to the ISO 13485 QMS standard.
On September 21, 2023, the Company announced the successful debut of its Intelligent Fingerprinting Drug Screening System at $8.50Australia’s only workplace health and safety event – the Work Place Health and Safety Show in Sydney.
 59,782On September 8, 2023, the Company announced the successful completion of Series B warrants exercisable at $0 (subjecta key development milestone in its plans to a cashless exercise provision)
2,363,003add ketamine and tramadol to its Intelligent Fingerprinting Drug Screening System. New assays for testing both drugs have passed the Company’s initial design phase and are ready for scale-up and transfer to manufacture in preparation for potential clinical trials. After completing these activities and successful clinical trials, the assays can be added to the panel of Series C Convertible Preferred Stocksubstances detected by the Company’s proprietary drug screening system.
 63,529 of Warrants issued to the underwriter exercisable at $18.70
 2,736,675On August 1, 2023, the Company announced that it had secured 8 new customers across various locations throughout Australia, which collectively employ over 10,000 individuals, within just two months of the Pre-IPO Warrants exercisable at $8.50 (during year two through year three after the IPO)launching its Intelligent Fingerprinting Drug Screening System in Australia.
 3,000,000 Warrants issued to LSBD exercisable at $17.00On July 6, 2023, the Company announced that it has signed a distribution agreement with Chile-based company TSCOM SPA for its Intelligent Fingerprinting Drug Screening System, increasing the product’s availability across South America. The Company further announced that it received its first order under this agreement, from a Chile-based electrical distribution company.

 

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Nasdaq Minimum Bid Price Requirement

On March 17, 2022, the Company received a letter (the “Notice”) from the Listing Qualifications Department of The Nasdaq Stock Market LLC (“Nasdaq”) notifying the Company that the minimum closing bid price per share for its common stock was below $1.00 for 30 consecutive business days preceding the date of the Notice, and that the Company did not meet the $1.00 per share minimum bid price requirement set forth in Nasdaq Listing Rule 5450(a)(1).

The Notice has no immediate effect on the listing or trading of the Company’s common stock on the Nasdaq Capital Market.

 

Pursuant to Nasdaq Listing Rule 5810(c)(3)(A), the Company had a compliance period of 180 calendar days, or until September 13, 2022 (the “Compliance Period”), to regain compliance with Nasdaq’s minimum bid price requirement. If at any time during the Compliance Period, the closing bid price per share of the Company’s common stock is at least $1.00 for a minimum of 10 consecutive business days, Nasdaq will provide the Company a written confirmation of compliance and the matter will be closed. On September 8, 2022, the Company filed a request for a second 180-day period within which to evidence compliance with the $1.00 bid price requirement following the expiration of the current compliance period on September 13, 2022. No further communication has been received from by Nasdaq as at the date of this Quarterly Report on Form 10-Q.

As part of its review process, Nasdaq will make a determination of whether it believes the Company will be able to cure the deficiency. If Nasdaq concludes that the Company will not be able to cure the deficiency, or if the Company determine not to submit a transfer application or make the required representation, Nasdaq will provide notice that the Company’s securities will be subject to delisting. If the Company chooses to implement a reverse stock split, it must complete the split no later than ten business days prior to the expiration of the second compliance period.

Results of Operations:Operations

 

Comparison of the Three Months Ended September 30, 20222023 and 20212022

  Three Months Ended September 30, 
  2023  2022 
Revenue $796,094  $- 
Cost of revenue (exclusive of amortization shown separately below)  (563,763)  - 
Gross profit  232,331   - 
         
Other income:        
Government support income  109,871   311,320 
         
Operating expenses:        
Selling, general and administrative expenses  (2,457,060)  (1,450,418)
Development and regulatory approval expenses  (103,947)  (79,274)
Depreciation and amortization  (307,560)  - 
Total operating expenses  (2,868,567)  (1,529,692)
Loss from operations  (2,526,365)  (1,218,372)
         
Other income (expense):        
Interest expense  (37,448)  (1,065)
Realized foreign exchange loss  -   (2,247)
Fair value gain on revaluation of financial instrument  131,250   - 
Interest income  139   7,606 
Total other income  93,941-   4,294 
Net loss  (2,432,424)  (1,214,078)
Net loss attributable to non-controlling interest  (7,220)  (5,785)
Net loss attributable to Intelligent Bio Solutions Inc. $(2,425,204) $(1,208,293)
         
Other comprehensive loss, net of tax:        
Foreign currency translation loss $(18,016) $(135,559)
Total other comprehensive loss  (18,016)  (135,559)
Comprehensive loss  (2,450,440)  (1,349,637)
Comprehensive loss attributable to non-controlling interest  (7,220)  (5,785)
Comprehensive loss attributable to Intelligent Bio Solutions Inc. $(2,443,220) $(1,343,852)
         
Net loss per share, basic and diluted* $(1.04) $(1.62)
Weighted average shares outstanding, basic and diluted*  2,330,399   744,495 

*Common Stock and per share amount have been retroactively adjusted to reflect the decreased number of shares resulting from a 1 for 20 reverse stock split effected on February 9, 2023, throughout the consolidated financial statement unless otherwise stated.

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Revenue

Sales of goods

Revenue from sales of goods increased from $0 to $796,094 for the quarter ended September 30, 2023, compared to same period in 2022. This is due to acquisition of IFP in October 2022, whose results of operations are consolidated, as well as, the launch of fingerprint drug testing in APAC region via Intelligent Bio Solutions (APAC) Pty Ltd. The acquisition provided the Company with access to a commercially available Fingerprinting drug testing system which is currently being marketed in Europe and the Asia Pacific Region.

Revenue from the IFPG segment relates to the sale of readers, cartridges and accessories and is summarized as follows:

  Three Months Ended September 30, 
  2023  2022 
Sales of goods - cartridges $380,059  $ 
Sales of goods - readers  238,802    
Other sales  177,233    
Total revenue $796,094  $ 

Cost of revenue

Cost of revenue increased by $563,763 to $563,763 from $0 for the quarter ended September 30, 2023, compared to same period in 2022. Cost of revenue relates to the direct labor, direct material costs and direct overhead costs incurred in the production of the goods.

Gross profit

Gross profit is primarily attributable to the IFPG segment. Gross profit increased from $0 to $232,331 for the quarter ended September 30, 2023, compared to same period in 2022. This is due to the acquisition of IFP in October 2022.

 

Government support income

 

Government support income increaseddecreased by $201,449 to $109,871 from $0 to $311,320 for the quarter ended September 30, 2022,2023, compared to same period in 2021. 2022. This decrease was primarily attributable to the timing of amount spent on qualifying research and development expenditure.

The grant support income is comprised of $250,907 as R&D tax refund and $60,413 as unwinding of deferred grant income for which the grant is intended to compensate. This increase was primarily attributable to INBS’s subsidiary companies recognizing $250,907 asan R&D tax refund on qualifying research and development expenditures during the three months ended September 30, 2022 as the Company believes that it is probable that the certain amount will be recovered in full through a future claim (see the R&D tax refund section of Note 3 to the unaudited condensedour consolidated financial statements includedappearing elsewhere in “Part I, Item 1 — Financial Statements” of this Quarterly Report on Form 10-Q for further information and incorporated herein by reference)disclosures relating R&D tax refund).

21

 

Operating expenses

 

GeneralSelling, general and administrative expenses

 

GeneralSelling, general and administrative expenses increased by $117,898$1,006,642 to $1,450,418$2,457,060 from $1,332,520$1,450,418 for the quarter year ended September 30, 2022,2023, compared to the same period in 2021.2022. This increase was primarily driven by an increaseis largely due to the acquisition of IFP which added approximately 32 staff to our FTE headcount, and the results of operations of IFP which are consolidated in operational activities following completionthe current period from the date of the IPO in December 2020.acquisition.

 

As the Company’s operating activities increase, we expect itsselling, general and administrative costs will include additional costs in overhead contribution, consultancy, as well as an increase in employee relatedemployee-related costs associated with a higher headcount.

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Development and regulatory expenses

 

Development and regulatory expenses decreasedincreased by $27,525$24,673 to $79,274$103,947 from $106,799$79,274 for the quarter ended September 30, 2022,2023, compared to the same period in 2021.2022. This decreaseincrease is primarily driven by the timing of invoicing for milestones/and research and development activities carried on at theout by University of Newcastle and other research partners.New Castle.

 

As the Company’s operating activities increase, we expect its development and regulatory expenses to increase in future periods.

 

Depreciation and amortization

Depreciation and amortization increased from $0 to $307,560 for the quarter ended September 30, 2023, compared to same period in 2022. This is due to the acquisition of IFP and primarily related to the amortization of acquired Intangibles and property and equipment acquired in October 2022.

Other income and expenses

 

Interest expense

 

Interest expense increased by $36,383 to $37,448 from $0 to $1,065 for the quarter ended September 30, 2022,2023, as compared to the same period in 2021.2022. This increase was attributable to the payment arrangementinterest expense recorded for directorsleased assets and officers insurance policy.notes payable.

 

Realized foreign exchange loss

 

Realized foreign exchange loss decreased by $871$2,247 to $2,247$0 from $3,118a loss of $2,247 for the quarter ended September 30, 2022,2023, compared to the same period in 2021.fiscal 2022. This decrease in loss was largely attributable to the favorable exchange rates while settling transactions in currencies other than its functional currencies.

 

Fair value gain on revaluation of financial instruments

The fair value gain on revaluation of financial instruments increased by $131,250 to $131,250 from $0 for the three months ended September 30, 2023, as compared to the same period in 2022. This increase is due to the revaluation gains on the contingent consideration for holdback shares resulting from the acquisition of IFP.

Income tax (expense) benefit

 

There was no income tax expense for both the three months period ended September 30, 2022,2023, and 2021,2022, respectively, as the Company has established a full valuation allowance for all its deferred tax assets.

 

Other comprehensive income

 

Foreign currency translation gain/(loss)

 

Unrealized foreign currency translation loss increaseddecreased by $68,077$117,543 to a loss of $135,559$18,016 from a loss of $67,482$135,559 for the quarter ended September 30, 2022,2023, compared to the same period in 2021.2023. It is calculated based on the Company’s unsettled transactions in currencies other than its functional currency and translation of assets and liabilities of foreign subsidiaries in reporting currency.

 

Net loss

 

Net loss attributable to INBS decreasedthe Company increased by $224,359$1,216,911 to $1,208,293$2,425,204 from $1,432,652$1,208,293 for the quarter ended September 30, 2022,2023, compared to the same period in 2021.2022. This decrease in lossincrease is primarily due todriven by combined results of operations after the acquisition of IFP offset by a recognition of government support income infair value gain on revaluation of holdback Series C Preferred Stock during the current quarter due to expenditure incurred on qualifying research and development activities.of $131,250.

 

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Liquidity and Capital Resources

We use working capital and cash measures to evaluate the performance of our operations and our ability to meet our financial obligations. We define Working Capital as current assets less current liabilities. This measure should not be considered in isolation or as a substitute for any standardized measure under GAAP. This information is intended to provide investors with information about our liquidity. Other companies in our industry may calculate this measure differently than we do, limiting its usefulness as a comparative measure.

 

Since our inception, our operations have primarily been financed through the issuance of our common stock, redeemable convertible preferred stock, and the incurrence of debt. As of September 30, 2022,2023, we had $5,742,626$186,401 in cash and cash equivalents and $5,850,203 ina working capital.capital deficit of $4,154,043.

 

See “Initial public offering & share structure” herein for details about our IPO.

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The Company expects that its cash and cash equivalents as of September 30, 2022, may2023, will be insufficient to allow the Company to fund its current operating plan through at least the next twelve months from the issuance of these financial statements, taking into account the acquisition of Intelligent Fingerprinting Limited. Should revenue not be generated during this period to cover expenses, then thesestatements. These conditions may raise substantial doubt about the Company’s ability to continue as a going concern for a period of at least one year from the date these financial statements are issued. It appears that the Company will be required to raise additional funds during the next 12 months. The Company is currently evaluating potential raising additional funds through private placements and or public equity financing. However, thereThere can be no assurance that, in the event that the Company requires additional financing, such financing will be available on terms which are favorable to us, or at all. Accordingly, these factors raise substantial doubt about the Company’s ability to continue as a going concern.

 

We do not anticipate generating any revenue inOn October 4, 2023, subsequent to the near future, until such time, if at all,quarter ended September 30, 2023, the Company completes the development process of its products, including regulatory approvals,raised approximately $4.378 million prior to deducting underwriting discounts and thereafter, begins to commercializecommissions and achieve substantial acceptance in the marketplace for the first ofoffering expenses via a series of products in its medical device portfolio. In addition, available resources may be consumed more rapidly than currently anticipated, and there can be no assurance that we will be successful in developing the SGT and generating sufficient revenue in the timeframe set forth above, or at all. We may be unable to meet our targets for regulatory approval and market launch, or we may be unable to generate anticipated amounts of revenue from salesregistered underwritten public offering of the system. We may also need additional fundingCompany’s securities. Net proceeds to the Company, after deducting the underwriting discounts and commissions and estimated offering expenses payable by the Company, were approximately $3.35 million. Refer to Note 15 for developing new products and services and for additional sales, marketing and promotional activities. Should this occur, we may need to seek additional capital earlier than anticipated.details.

 

In the event we require additional capital, there can be no assurances that we will be able to raise such capital on acceptable terms, or at all. Failure to generate sufficient revenues or raise additional capital through debt or equity financings, or through collaboration agreements, strategic alliances or marketing and distribution arrangements, could have a material adverse effect on our ability to meet our long-term liquidity needs and achieve our intended long-term business plan. Our failure to obtain such funding when needed could create a negative impact on our stock price or could potentially lead to a reduction in our operations or the failure of our company. Accordingly, these factors raise substantial doubt about the Company’s ability to continue as a going concern.concern unless it can successfully raise additional capital.

 

Extended Transition Period for “Emerging Growth Companies”

 

We have elected to use the extended transition period for complying with new or revised accounting standards under Section 102(b)(1) of the JOBS Act. This election allows us to delay the adoption of new or revised accounting standards that have different effective dates for public and private companies until those standards apply to private companies. As a result of this election, our financial statements may not be comparable to companies that comply with public company effective dates. Because our financial statements may not be comparable to companies that comply with public company effective dates, investors may have difficulty evaluating or comparing our business, performance or prospects in comparison to other public companies, which may have a negative impact on the value and liquidity of our common stock.

 

Critical Accounting Estimates

 

The preparation of our consolidated financial statements in conformity with GAAP requires management to make judgments, estimates and assumptions that impact the amounts reported in our consolidated financial statements and accompanying notes that are not readily apparent from other sources. The estimates and associated assumptions are based on historical experience and other factors that are considered relevant. Actual results may differ from these estimates.

 

30

Our critical

The estimates and underlying assumptions are reviewed on an ongoing basis. Revisions to accounting estimates are recognized in the period in which the estimate is revised, if the revision affects only that period, or in the period of the revision and future periods, if the revision affects both current and future periods.

A summary of our significant accounting policies is included in Note 3 “Summary of significant accounting policies” to the accompanying unaudited condensed consolidated financial statements. Certain of our accounting policies are describedconsidered critical, as these policies require significant, difficult or complex judgments by management, often requiring the use of estimates about the effects of matters that are inherently uncertain. Our critical policies are summarized in Item 7. “Management’s Discussion and Analysis of Financial Condition and Results of Operations” of our Annual Report on Form 10-K filed withfor the SEC on September 22, 2022, and the notes to the unaudited condensed consolidated financial statements included in “Part I, Item 1 — Financial Statements” of this Quarterly Report on Form 10-Q.year ended June 30, 2023.

 

During the three months ended September 30, 2022, there were no material changes to our critical accounting policies from those in our June 30, 2022, Annual Report on Form 10-K filed with the SEC on September 22, 2022.

Recently issued Accounting Pronouncements

 

For the impact of recently issued accounting pronouncements on the Company’s unaudited condensed consolidated financial statements, see Note 3 to the unaudited condensed consolidated financial statements included in “PartPart I, Item 1 — Financial Statements” of this Quarterly Report on Form 10-Q and incorporated herein by reference.

 

Off-balance sheet arrangements

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As of September 30, 2023, and June 30, 2023, we did not have any off-balance sheet arrangements.

 

ITEM 3. QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK.

 

We are a smaller reporting company as defined by Rule 12b-2 of the Exchange Act and are not required to provide the information otherwise required under this item.

 

ITEM 4. CONTROLS AND PROCEDURES

 

Evaluation of Disclosure Controls and Control Procedures

 

Our management, with the participation of our Principal Executive Officer and Principal Financial and Accounting Officer, evaluated the effectiveness of our disclosure controls and procedures as of September 30, 2023. The term “disclosure controls and procedures,” as defined in Rules 13a-15(e) and 15d-15(e)) under the designSecurities Exchange Act, as amended (the “Exchange Act”), means controls and operationsother procedures of a company that are designed to ensure that information required to be disclosed by a company in the reports that it files or submits under the Exchange Act is recorded, processed, summarized and reported within the time periods specified in the SEC’s rules and forms. Disclosure controls and procedures include, without limitation, controls and procedures designed to ensure that information required to be disclosed by a company in the reports that it files or submits under the Exchange Act is accumulated and communicated to the company’s management, including its principal executive and principal financial officers, as appropriate to allow timely decisions regarding required disclosure. Management recognizes that any controls and procedures, no matter how well designed and operated, can provide only reasonable assurance of achieving their objectives and management necessarily applies its judgment in evaluating the cost-benefit relationship of possible controls and procedures.

Based on the evaluation of our disclosure controls and procedures (as defined in Rules 13a-15(e) and 15d-15(e) under the Exchange Act) as of the end of the period covered by this Quarterly Report on Form 10-Q,September 30, 2023, our Chief Executive Officer and haveChief Financial Officer concluded that, based onas of such evaluation,date, our disclosure controls and procedures were not effectiveineffective due to the material weaknesses in our internal control over financial reporting as of September 30, 2022 as described below.

A material weakness is a deficiency, or a combination of deficiencies, in internal control over financial reporting such that there is a reasonable possibility that a material misstatement of a company’s annual or interim consolidated financial statements will not be prevented or detected on a timely basis.discussed below.

Notwithstanding thethis conclusion, that our disclosure controls and procedures were not effective as of the end of the period covered by this report, we believe that our unaudited condensedconsolidated financial statements and other information contained in this Quarterly Reportquarterly report on Form 10-Q present fairly, in all material respects, our business, financial condition and results of operations for the interim periods presented.

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Material Weaknesses

 

As a resultIn its assessment of the assessment, management concluded that the Company’seffectiveness of internal control over financial reporting was ineffective as of the evaluation date due to the followingJune 30, 2023, management identified material weaknesses in control environment, risk assessment, control activities, information and communication and monitoring.

The Specifically, the material weaknesses identified relate to the fact that the Company has not yet designed and maintained an effective control environment commensurate with its financial reporting requirements, including a)(a) has not yet completed the formally documented policies and procedures with respect to the review, supervision and monitoring of the Company’s accounting and reporting functions, b)(b) lack of evidence to support the performance of controls and the adequacy of review procedures, including the completeness and accuracy of information used in the performance of controls and c)(c) as an emerging growth company we currently have limited accounting personnel and other supervisory resources necessary to adequately execute the Company’s accounting processes and address its internal controls over financial reporting.

Remediation Plan

 

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Remediation Plan

Management is committed to continuing with the steps necessary to remediate the control deficiencies that constituted the above material weaknesses. Since the IPO, our initial public offering (“IPO”), which we completed in December 2020, we made the following enhancements to our control environment:

 

● We added accounting and finance personnel to provide additional individuals to allow for segregation of duties in the preparation and review of schedules, calculations, and journal entries that support financial reporting, to provide oversight, structure and reporting lines, and to provide additional review over our disclosures;

● We enhanced our controls to improve the preparation and review over complex accounting measurements, and the application of GAAP to significant accounts and transactions, and our financial statement disclosures; and,

● We engage independent experts when complex transactions are entered into;

● We plan to recruit additional financial reporting and accounting personnel with adequate knowledge of US GAAP and SEC rules; and

● We are in the process of engaging outside consultants to assist us in our evaluation of the design, implementation, and documentation of internal controls that address the relevant risks, and that provide for appropriate evidence of performance of our internal controls (including completeness and accuracy procedures).

 

We added accounting and finance personnel to provide additional individuals to allow for segregation of duties in the preparation and review of schedules, calculations, and journal entries that support financial reporting, to provide oversight, structure and reporting lines, and to provide additional review over our disclosures;
We enhanced our controls to improve the preparation and review over complex accounting measurements, and the application of GAAP to significant accounts and transactions, and our financial statement disclosures;
We plan to engage independent experts when complex transactions are entered;
We plan to recruit additional financial reporting and accounting personnel with adequate knowledge of US GAAP and SEC rules; and
We are in the process of engaging outside consultants to assist us in our evaluation of the design, implementation, and documentation of internal controls that address the relevant risks, and that provide for appropriate evidence of performance of our internal controls (including completeness and accuracy procedures).

Under the direction of the audit committeeAudit Committee of our board of directors, management will continue to take measures to remediate the material weakness in the fiscal year 2023.weaknesses. As such, we will continue to enhance corporate oversight over process-level controls and structures to ensure that there is appropriate assignment of authority, responsibility, and accountability to enable remediation of our material weakness.

 

As we continue to evaluate, and work to improve, our internal control over financial reporting, management may determine that additional measures to address control deficiencies or modifications to the remediation plan are necessary.

 

Changes in Internal Control Over Financial Reporting

Other than the ongoing remediation effort, described above, there have been no changes to the Company’s internal controls over financial reporting (as defined in Rules 13a-15(f) and 15d 15(f) under the Exchange Act) during the most recent fiscal quarter that have materially affected, or are reasonably likely to materially affect, our internal control over financial reporting.

On October 4, 2022, the Company completed the acquisition of IFP. In accordance with the guidance issued by the SEC, recently acquired businesses may be excluded from management’s assessment of the effectiveness of the Company’s internal control over financial reporting for up to a year from the date of acquisition and from the annual management report on internal control over financial reporting for the year of acquisition. Accordingly, management excluded the IFP Acquisition from the management’s assessment of the effectiveness of the Company’s internal control over financial reporting from October 4, 2022 (the acquisition date), which excluded total assets and total net revenue representing approximately 82.64% and 99% respectively, of the Company’s related consolidated financial statement amounts as of and for quarter ended September 30, 2023.

 

Inherent Limitation on the Effectiveness of Internal Controls

 

The effectiveness of anyA control system, of internal control over financial reporting, including ours, is subject to inherent limitations, including the exercise of judgment in designing, implementing, operating, and evaluating the controls and procedures, and the inability to eliminate misconduct completely. Accordingly, in designing and evaluating the disclosure controls and procedures, management recognizes that any system of internal control over financial reporting, including ours, no matter how well designedconceived and operated, can provide only provide reasonable, not absolute, assurance that the objectives of achieving the desiredinternal control objectives. In addition,system are met. Because of the design of disclosure controls and procedures must reflect the fact that there are resource constraints, and that management is required to apply its judgment in evaluating the benefits of possible controls and procedures relative to their costs. Moreover, projectionsinherent limitations of any internal control system, no evaluation of effectiveness to future periods are subject to the riskcontrols can provide absolute assurance that controls may become inadequate because of changes in conditions, or that the degree of compliance with the policies or procedures may deteriorate. We intend to continue to monitor and upgrade our internal controls as necessary or appropriate for our business but cannot assure you that such improvements will be sufficient to provide us with effective internalall control over financial reporting.issues, if any, within a company have been detected.

 

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PART II. OTHER INFORMATION

ITEM 1. LEGAL PROCEEDINGS.

From time to time, we may be subject to legal proceedings and claims arising in the ordinary course of business. We are not currently engaged in any material legal proceedings.

ITEM 1A. RISK FACTORS.

As of the date of this Quarterly Report on Form 10-Q, there have been no material changes to the risk factors disclosed in our Annual Report on Form 10-K filed with the SEC on September 22, 2022August 23, 2023, except for the risks described below. Any of those risk factors could result in a significant or material adverse effect on our results of operations or financial condition. Additional risk factors not presently known to us or that we currently deem immaterial may also impair our business or results of operations. We may disclose changes to such factors or disclose additional factors from time to time in our future filings with the SEC.

 

We will need to raise additional capital to fund our operations in the future. If we are unsuccessful in attracting new capital, we may not be able to satisfycontinue operations or may be forced to sell assets to do so. Alternatively, capital may not be available to us on favorable terms, or if at all. If available, financing terms may lead to significant dilution of our stockholders’ equity.

We are not profitable and have had negative cash flow from operations since our inception. To fund our operations and develop and commercialize our products (including the continued listing requirementsSGT and planned applications of IFP Drug Screening System), we have relied primarily on equity and debt financings and government support income. The Company expects that its cash and cash equivalents as of September 30, 2023, of $186,401, will be insufficient to allow the Company to fund its current operating plan through at least the next twelve months from the issuance of its unaudited condensed consolidated financial statements for the fiscal quarter ended September 30, 2023. These conditions raise substantial doubt about the Company’s ability to continue as a going concern for a period of at least one year from the date these unaudited condensed consolidated financial statements were issued. Accordingly, the Company will be required to raise additional funds during the next 12 months. However, there can be no assurance that when the Company requires additional financing, such financing will be available on terms which are favorable to the Company, or at all. If the Company is unable to raise additional funding to meet its working capital needs in the future, it will be forced to delay or reduce the scope of its research programs and/or limit or cease its operations. In addition, the Company may be unable to realize its assets and discharge its liabilities in the normal course of business.

Accordingly, these factors raise substantial doubt about the Company’s ability to continue as a going concern unless it can successfully raise additional capital. On October 4, 2023, subsequent to the quarter ended September 30, 2023, the Company raised approximately $4.378 million prior to deducting underwriting discounts and commissions and offering expenses via a registered underwritten public offering of the Nasdaq Capital MarketCompany’s securities. Net proceeds to the Company, after deducting the underwriting discounts and commissions and estimated offering expenses payable by the Company, were approximately $3.35 million.

To obtain the capital necessary to fund our operations, we expect to finance our cash needs through public or private equity offerings, debt financing and/or other capital sources. Even if capital is available, it might be available only on unfavorable terms. Any additional equity or convertible debt financing into which we enter could be dilutive to our existing stockholders. Any future debt financing into which we enter may impose covenants upon us that restrict our operations, including limitations on our ability to incur liens or additional debt, pay dividends, repurchase our stock, make certain investments and engage in ordercertain merger, consolidation or asset sale transactions. Any debt financing or additional equity that we raise may contain terms that are not favorable to us or our stockholders. If we raise additional funds through collaboration and licensing arrangements with third parties, we may need to relinquish rights to our technologies or our products or grant licenses on terms that are not favorable to us. If access to sufficient capital is not available as and when needed, our business will be materially impaired, and we may be required to cease operations, curtail one or more product development or commercialization programs, scale back or eliminate the development of business opportunities, or significantly reduce expenses, sell assets, seek a merger or joint venture partner, file for protection from creditors or liquidate all of our assets. Any of these factors could harm our operating results.

33

We have identified material weaknesses in our internal control over financial reporting. If our remediation of the material weaknesses is not effective, or if we experience additional material weaknesses in the future or otherwise fail to maintain an effective system of internal controls in the listingfuture, we may not be able to accurately or timely report our financial condition or results of operations, which may adversely affect investor confidence in us and, as a result, the value of our common stock.

 

On March 17, 2022,In connection with the Company receivedpreparation of our financial statements for the fiscal year ended June 30, 2023, we identified material weaknesses in our internal control over financial reporting. A material weakness is a letter (the “Notice”) from the Listing Qualifications Departmentdeficiency, or combination of The Nasdaq Stock Market LLC (“Nasdaq”) notifying the Companydeficiencies, in internal controls such that the minimum closing bid price per share for its common stock was below $1.00 for 30 consecutive business days preceding the datethere is a reasonable possibility that a material misstatement of the Notice, and that the Company didour financial statements will not meet the $1.00 per share minimum bid price requirement set forth in Nasdaq Listing Rule 5450(a)(1).be prevented or detected on a timely basis.

 

The Noticematerial weaknesses related to the fact that the Company has no immediate effect onnot yet designed and maintained an effective control environment commensurate with its financial reporting requirements, including (a) that the listing or tradingCompany had not yet completed the formally documented policies and procedures with respect to the review, supervision and monitoring of the Company’s common stock onaccounting and reporting functions, (b) the Nasdaq Capital Market.lack of evidence to support the performance of controls and the adequacy of review procedures, including the completeness and accuracy of information used in the performance of controls and (c) as an emerging growth company we currently have limited accounting personnel and other supervisory resources necessary to adequately execute the Company’s accounting processes and address its internal controls over financial reporting.

 

PursuantWe have implemented and are in the process of implementing measures designed to Nasdaq Listing Rule 5810(c)(3)(A),improve our internal control over financial reporting to remediate these material weaknesses, including the Company had a compliance periodhiring of 180 calendar days, or until September 13, 2022 (the “Compliance Period”),additional qualified accounting and finance personnel, enhancing our controls to regain compliance with Nasdaq’s minimum bid price requirement. If at any time duringimprove the Compliance Period, the closing bid price per share of the Company’s common stock is at least $1.00 for a minimum of 10 consecutive business days, Nasdaq will provide the Company a written confirmation of compliancepreparation and review over complex accounting measurements and the matter will be closed.application of GAAP, and engaging independent experts and outside consultants.

 

On September 8, 2022,We cannot assure you that the Company filedmeasures we have taken and that we intend to take will be sufficient to remediate the material weaknesses we have identified or avoid potential future material weaknesses. While we believe that our efforts will enhance our internal control, remediation of the material weaknesses will require further validation and testing of the design and operating effectiveness of internal controls over a requestsustained period of financial reporting cycles, and we cannot assure you that we have identified all, or that we will not in the future have additional, material weaknesses.

The sale of a substantial number of shares of our common stock and other securities convertible into or exercisable for our common stock, such as those securities sold in the October 2023 Offering, could depress the market price of our shares of common stock and impair our ability to raise capital through the sale of additional equity securities.

The shares of common stock and Series E Convertible Preferred Stock (which is convertible into common stock) sold in the October 2023 Offering more than doubled the number of shares of our common stock in the public market from approximately 2,330,399 shares to 10,291,343 shares (including 5,728,723 shares Series E Preferred Stock convertible into common stock). If all the warrants sold in the October 2023 Offering are exercised, the number of shares of our common stock in the public markets will increase by an additional 15,921,888 shares, which will result in a second 180-day period within whichtotal of 26,231,231 shares of our common stock in the public market. In addition, we agreed to evidence complianceissue warrants to the representative of the underwriters in the October 2023 Offering (the October Representative Warrants) to purchase up to 398,047 shares of common stock as a portion of the compensation payable to the representative in connection with the $1.00 bidOctober 2023 Offering. The sales of these securities could depress the market price requirement followingof our shares of common stock and/or increase the expirationvolatility of our trading.

The sale of a substantial number of shares of our common stock and other securities convertible into or exercisable for our common stock, such as those securities sold in the current compliance periodOctober 2023 Offering, could depress the market price of our shares of common stock and impair our ability to raise capital through the sale of additional equity securities. In addition to causing the market price of our common stock to decline, such sales could also greatly increase the volatility associated with the trading of our common stock. Furthermore, stockholders may initiate securities class action lawsuits if the market price of our common stock drops significantly, which may cause us to incur substantial costs and could divert the time and attention of our management. We cannot predict the number of these shares or warrants that might be sold nor the effect that future sales of our shares of our securities would have on September 13, 2022. No further communication has been received from by Nasdaq as at the datemarket price of this Quarterly Report on Form 10-Q.

26

our shares of common stock.

As part of its review process, Nasdaq will make a determination of whether it believes the Company will be able to cure the deficiency. If Nasdaq concludes that the Company will not be able to cure the deficiency, or if the Company determine not to submit a transfer application or make the required representation, Nasdaq will provide notice that the Company’s securities will be subject to delisting. If the Company chooses to implement a reverse stock split, it must complete the split no later than ten business days prior to the expiration of the second compliance period.

Our Licensor is undergoing equity recapitalizationIf we are unable to achieve certain agreed milestones for the outcomegovernment grant we received, we may become liable to refund the grant we received. The Company has only completed 4 of the 8 agreed milestones set forth in the Company’s grant agreement with which could materially and adversely affect our business, financial condition and operating results.the Australian Government.

 

We are party to a Technology License Agreement (the “Technology License Agreement”) with Life Science Biosensor Diagnostics Pty Ltd. (“LSBD”), pursuant to which, among other things,As of September 30, 2023, there is uncertainty regarding the Company licenses certain products from LSBD (the “Licensed Products”), and an option agreement with LSBD and BiosensX (North America) Inc., pursuant to which, among other things, LSBD granted to the Company an exclusive option (the “Option”) to purchase an exclusive license to use, make, sell and offer to sell products under the intellectual property rights in connection with the Biosensor technology the glucose/diabetes management field in the United States, Mexico and Canada. See exhibits 10.2, exhibits 10.3, exhibits 9, 5– Technology License Agreementspotential extension of the 10-K filedgrant agreement past its original end date of March 28, 2024. If we are not given an extension beyond the original end date, or if we are unable to achieve the agreed milestones on September 22, 2022 for a description oftime, we may become liable to refund the Technology License Agreement, the Licensed Products, and the Option. According to the Australian Securities and Investment Commission’s (ASIC’s), Companies and Organizations Register, on May 10, 2022, LSBD filed a Notice of Appointment of External Administrator, followed by a filing of a Deed of Company Arrangement on the August 2, 2022. Pursuant this filinggrant we understand that LSBD is proposing to undergo a recapitalization of its equity structure on or before December 5, 2022. We understand, the Deed Administrators granted a further extension from October 2, 2022 to December 5, 2022 to the Deed Proponents to complete their due diligence. The terms of such recapitalization or other outcome of such administration of LSBD could result in, among other things, change in control of the Licensor or more parties other than LSBD becoming the owner of the Intellectual Property (IP) rights. Accordingly, this has an inherent risk of the possibility of modifications to, or the Company’s ability to use, the Licensed Products, which could materially and adversely affect the Company’s business, financial condition and operating results.received.

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

Other than any sales previously reported in the Company’s Current Reports on Form 8-K, the Company did not sell any unregistered securities during the period covered by this report.

 

ITEM 3. DEFAULTS UPON SENIOR SECURITIES.

None.

 

ITEM 4. MINE SAFETY DISCLOSURES.

Not applicable.

 

ITEM 5. OTHER INFORMATION.

None.

 

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ITEM 6. EXHIBITS

Exhibit No. Description
2.1 
3.1Share Exchange Agreement, dated asCertificate of October 4, 2022, by and among GBS INC., Intelligent Fingerprinting Limited, the Sellers Listed on Schedule I thereto, Jason Isenberg (as the RFA Sellers’ Representative), and Philip Hand (as the other Sellers’ Representative)Elimination of Series B Convertible Preferred Stock (incorporated by reference to Exhibit 2.13.1 to the Company’s Current Report on Form 8-K filed with the Commission on October 11, 2022)July 26, 2023).
3.13.2 Certificate of Elimination of Series D Convertible Preferred Stock (incorporated by reference to Exhibit 3.2 to the Company’s Current Report on Form 8-K filed with the Commission on July 26, 2023).
3.3Certificate of Designation of Preferences, Rights and Limitations of the Series CE Convertible Preferred Stock, par value $0.01 per share, of the Company, dated October 4, 2022, filed with the Delaware Secretary of State of Delaware on October 4, 20223, 2023 (incorporated by reference to Exhibit 3.1 to the Company’s Current Report on Form 8-K filed with the Commission on October 11, 2022)4, 2023).
3.24.1 CertificateForm of Amendment to the Amended and Restated Certificate of Incorporation of GBS Inc. (now known as Intelligent Bio Solutions Inc.), as filed with the Secretary of State of Delaware on October 26, 2022Series E Warrant (incorporated by reference to Exhibit 3.14.1 to the Company’s Current Report on Form 8-K filed with the Commission on October 27, 2022)4, 2023).
3.34.2 FAmended and Restated Bylawsorm of Intelligent Bio Solutions Inc., as amended as of October 26, 2022Series F Warrant (incorporated by reference to Exhibit 3.24.2 to the Company’s Current Report on Form 8-K filed with the Commission on October 27, 2022)4, 2023).
10.14.3 Employment Agreement between the Glucose Biosensor Systems (Greater China) Pty Ltd and Spiro SakirisForm of Representative Warrant (incorporated by reference to Exhibit 10.1 to the Company’s Current Report on Form 8-K filed with the Commission on September 15, 2022)
10.2Employment Agreement between the Glucose Biosensor Systems (Greater China) Pty Ltd and Harry Simeonidis (incorporated by reference to Exhibit 10.2 to the Company’s Current Report on Form 8-K filed with the Commission on September 15, 2022)
10.3Employment Agreement between the GBS (APAC) Pty Ltd and Steven Boyages (incorporated by reference to Exhibit 10.1 to the Company’s Current Report on Form 8-K filed with the Commission on September 30, 2022).
10.4Investors’ Rights Agreement, dated as of October 4, 2022, by and among the Company, The Ma-Ran Foundation, The Gary W. Rollins Foundation and Jason Isenberg, as the RFA Sellers’ Representative (incorporated by reference to Exhibit 10.14.3 to the Company’s Current Report on Form 8-K filed with the Commission on October 11, 2022)4, 2023).
10.54.4 Registration RightsWarrant Agency Agreement, dated as of October 4, 2022, by2023, between Intelligent Bio Solutions Inc. and among theContinental Stock Transfer & Trust Company and the stockholders of the Company named therein (incorporated by reference to Exhibit 10.24.4 to the Company’s Current Report on Form 8-K filed with the Commission on October 11, 2022).
10.6Registration Rights Agreement, dated as of October 4, 2022, by and among the Company and the stockholders of the Company named therein (incorporated by reference to Exhibit 10.3 to the Company’s Current Report on Form 8-K filed with the Commission on October 11, 2022)2023).
10.7Voting Agreement, dated as of October 4, 2022, by and among the Company and the stockholders of the Company named therein (incorporated by reference to Exhibit 10.4 to the Company’s Current Report on Form 8-K filed with the Commission on October 11, 2022).
10.8Form of Voting Agreement, dated as of October 4, 2022, by and among the Company, the Sellers’ Representatives’ named therein and each of Spiro Sakiris, Harry Simeonides and Christopher Towers (incorporated by reference to Exhibit 10.5 to the Company’s Current Report on Form 8-K filed with the Commission on October 11, 2022).
10.9Extension Agreement, dated as of October 4, 2022, to Bridge Facility Agreement, dated as of June 16, 2022, between the Company and Intelligent Fingerprinting Limited (incorporated by reference to Exhibit 10.6 to the Company’s Current Report on Form 8-K filed with the Commission on October 11, 2022).
10.10Deed of Amendment and Restatement, dated October 4, 2022, between Intelligent Fingerprinting Limited, Karin Briden and the Company (incorporated by reference to Exhibit 10.7 to the Company’s Current Report on Form 8-K filed with the Commission on October 11, 2022).
10.11Deed of Amendment and Restatement, dated October 4, 2022, between Intelligent Fingerprinting Limited, Debra Coffey and the Company (incorporated by reference to Exhibit 10.8 to the Company’s Current Report on Form 8-K filed with the Commission on October 11, 2022).
10.12Deed of Amendment and Restatement, dated October 4, 2022, between Intelligent Fingerprinting Limited, Thomas Johnson and the Company (incorporated by reference to Exhibit 10.9 to the Company’s Current Report on Form 8-K filed with the Commission on October 11, 2022).
10.13Deed of Amendment and Restatement, dated October 4, 2022, between Intelligent Fingerprinting Limited, The Ma-Ran Foundation, The Gary W. Rollins Foundation and the Company (incorporated by reference to Exhibit 10.10 to the Company’s Current Report on Form 8-K filed with the Commission on October 11, 2022).
10.14Deed of Amendment and Restatement, dated October 4, 2022, between Intelligent Fingerprinting Limited, John Polden and the Company (incorporated by reference to Exhibit 10.11 to the Company’s Current Report on Form 8-K filed with the Commission on October 11, 2022).
10.15Deed of Amendment and Restatement, dated October 4, 2022, between Intelligent Fingerprinting Limited, Sennett Kirk III and the Company (incorporated by reference to Exhibit 10.12 to the Company’s Current Report on Form 8-K filed with the Commission on October 11, 2022).
10.16Deed of Amendment and Restatement, dated October 4, 2022, between Intelligent Fingerprinting Limited, Sennett Kirk III Exempt Trust and the Company (incorporated by reference to Exhibit 10.13 to the Company’s Current Report on Form 8-K filed with the Commission on October 11, 2022).
31.1# Certification of Principal Executive Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002.
31.2# Certification of Principal Financial Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002.
32.1# Certification of the Principal Executive Officer pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-OxleySarbanes- Oxley Act of 2002.
32.2# Certification of the Principal Financial Officer pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-OxleySarbanes- Oxley Act of 2002.
101.INS# Inline XBRL Instance Document.
101.SCH# Inline XBRL Taxonomy Extension Schema Document.
101.CAL# Inline XBRL Taxonomy Extension Calculation Linkbase Document.
101.DEF# Inline XBRL Taxonomy Extension Definition Linkbase Document.
101.LAB# Inline XBRL Taxonomy Extension Label Linkbase Document.
101.PRE# Inline XBRL Taxonomy Extension Presentation Linkbase Document.
104# Cover Page Interactive Data File (formatted in XBRL and included in Exhibit 101).

# Filed herewith.

 

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SIGNATURES

 

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

 

 Intelligent Bio Solutions Inc.
   
Date:November 10, 20228, 2023By:/s/ Harry Simeonidis
  HARRY SIMEONIDIS
  CHIEF EXECUTIVE OFFICER AND PRESIDENT
  (Principal Executive Officer)
   
Date:November 10, 20228, 2023By:/s/ Spiro Sakiris
  SPIRO SAKIRIS
  CHIEF FINANCIAL OFFICER
  (Principal Financial Officer)

 

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