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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM S-1
REGISTRATION STATEMENT UNDER THE SECURITIES ACT OF 1933
NETMED, INC.
(Exact name of registrant as specified in its charter)
Ohio 5047 31-1282391
(State or other jurisdiction of (Primary Standard Industrial (I.R.S. Employer
incorporation or organization) Classification Code Number Identification Number)
6189 Memorial Drive
Dublin, OH 43017
(614) 793-9356
(Address, including zip code, and telephone number,
including area code, of registrant's principal executive offices)
David J. Richards, President
NetMed, Inc.
6189 Memorial Drive
Dublin, OH 43017
(614) 793-9356
(Name, address, including zip code, and telephone number,
including area code, of agent for service)
Copies to:
William J. Kelly, Jr.
Vice President and General Counsel
NetMed, Inc.
6189 Memorial Drive
Dublin, OH 43017
(614) 793-9356
Approximate date of commencement of proposed sale to the public: As
soon as practicable after this Registration Statement becomes effective.
If any of the securities being registered on this Form are to be
offered on a delayed or continuous basis pursuant to Rule 415 under the
Securities Act of 1933, check the following box. [x]
If this Form is filed to register additional securities for an offering
pursuant to Rule 462(b) under the Securities Act, please check the following box
and list the Securities Act registration statement number of the earlier
effective registration statement for the same offering. [ ]
If this Form is a post-effective amendment filed pursuant to Rule
462(c) under the Securities Act, check the following box and list the Securities
Act registration statement number of the earlier effective registration
statement for the same offering. [ ]
If delivery of the prospectus is expected to be made pursuant to Rule
434, please check the following box. [ ]
CALCULATION OF REGISTRATION FEE
- ---------------------------------------------------------------------------------------------------------------------
TITLE OF EACH CLASS OF AMOUNT TO BE PROPOSED MAXIMUM PROPOSED MAXIMUM AMOUNT OF
SECURITIES TO BE REGISTERED AGGREGATE PRICE PER AMOUNT OF OFFERING REGISTRATION FEE
REGISTERED SHARE (1) PRICE (1) (1)
- ---------------------------------------------------------------------------------------------------------------------
Common Shares, without 1,500,000 $4.375 $6,562,500 $21,656.25
par value
- ---------------------------------------------------------------------------------------------------------------------
<FN>
(1) Calculated in accordance with Rule 457(c) based on the average of the high
and low sales prices of the Common Shares as reported on the American Stock
Exchange on September 11, 1997 solely for the purpose of calculating the
amount of the registration fee.
THE REGISTRANT HEREBY AMENDS THIS REGISTRATION STATEMENT ON SUCH DATE OR DATES
AS MAY BE NECESSARY TO DELAY ITS EFFECTIVE DATE UNTIL THE REGISTRANT SHALL FILE
A FURTHER AMENDMENT WHICH SPECIFICALLY STATES THAT THIS REGISTRATION STATEMENT
SHALL THEREAFTER BECOME EFFECTIVE IN ACCORDANCE WITH SECTION 8(a) OF THE
SECURITIES ACT OF 1933 OR UNTIL THE REGISTRATION STATEMENT SHALL BECOME
EFFECTIVE ON SUCH DATE AS THE COMMISSION, ACTING PURSUANT TO SAID SECTION 8(a),
MAY DETERMINE.
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PROSPECTUS
1,500,000 SHARES
NETMED, INC.
COMMON SHARES
(without par value)
The shares offered hereby (the "Shares") consist of up to 1,500,000
common shares, without par value (the "Common Stock") of NetMed, Inc., an Ohio
corporation ("NetMed" or the "Company") which are issuable by the Company to
certain persons ("Selling Shareholders") upon conversion of the 6% Convertible
Subordinated Debentures of the Company ("Debentures"), and upon exercise by the
Selling Shareholders of certain warrants to purchase Common Stock ("Warrants").
For further information regarding the Selling Shareholders, see "Selling
Shareholders." The number of shares registered for sale by this Prospectus
equals approximately 150% of the number of shares into which the Debentures are
convertible on September 10, 1997, assuming the Debentures were fully
convertible on such date, plus the number of Shares issuable upon exercise of
the Warrants. For a further description of the terms of the Debentures and the
Warrants, see "Selling Shareholders."
This Prospectus covers the sale of the Shares from time to time by the
Selling Shareholders. The issuance of Shares upon conversion of the Debentures
and exercise of the Warrants is not covered by this Prospectus, but rather only
the resale of such Shares. The Shares may be offered from time to time by the
Selling Shareholders. All expenses of the registration incurred in connection
herewith are being borne by the Company, but any brokers' or underwriters' fees
or commissions will be borne by the Selling Shareholders. The Company will not
receive any proceeds from the sale of the Shares by the Selling Shareholders.
The Selling Shareholders have not advised the Company of any specific
plans for the distribution of the Shares covered by this Prospectus, but it is
anticipated that the Shares will be sold from time to time primarily in
transactions (which may include block transactions) on the American Stock
Exchange at the market price then prevailing, although sales may also be made in
negotiated transactions or otherwise. The Selling Shareholders and the brokers
and dealers through whom sale of the Shares may be made may be deemed to be
"underwriters" within the meaning of the Securities Act of 1933, as amended (the
"Securities Act"), and their commissions or discounts and other compensation may
be regarded as underwriters' compensation. See "Plan of Distribution."
The Common Stock is currently listed on the American Stock Exchange
under the symbol "NMD." On September 11, 1997, the last reported sale price of
the Common Stock on the American Stock Exchange was $4.50 per share.
Application has been made to list the Shares on the American Stock Exchange.
THERE ARE CERTAIN RISK FACTORS THAT SHOULD BE CONSIDERED BEFORE
PURCHASING SHARES IN THIS OFFERING. SEE "RISK FACTORS."
THESE SECURITIES HAVE NOT BEEN APPROVED OR DISAPPROVED BY THE
SECURITIES AND EXCHANGE COMMISSION OR ANY STATE SECURITIES COMMISSION NOR HAS
THE COMMISSION OR ANY STATE SECURITIES COMMISSION PASSED UPON THE ACCURACY OR
ADEQUACY OF THIS PROSPECTUS. ANY REPRESENTATION TO THE CONTRARY IS A CRIMINAL
OFFENSE.
The date of this Prospectus is September __, 1997.
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AVAILABLE INFORMATION
This Prospectus, which constitutes a part of a Registration Statement
on Form S-1 (the "Registration Statement") filed by the Company with the
Securities and Exchange Commission (the "Commission") under the Securities Act,
omits certain of the information set forth in the Registration Statement.
Reference is hereby made to the Registration Statement and to the exhibits
thereto for further information with respect to the Company and the securities
offered hereby. Copies of the Registration Statement and the exhibits thereto
are on file at the offices of the Commission and may be obtained upon payment of
the prescribed fee or may be examined without charge at the public reference
facilities of the Commission described below.
Statements contained herein concerning the provisions of documents are
necessarily summaries of such documents, and each statement is qualified in its
entirety by reference to the copy of the applicable document filed with the
Commission.
The Company is subject to the informational requirements of the
Securities Exchange Act of 1934, as amended (the "Exchange Act") and in
accordance therewith files reports, proxy statements and other information with
the Commission. Such reports, proxy statements and other information can be
inspected and copied at the Public Reference Section of the Commission at 450
Fifth Street, N.W., Room 1024, Washington, D.C. 20549, and at the following
regional offices of the Commission: Midwest Regional Office, Citicorp Center,
500 West Madison Street, Suite 1400, Chicago, IL 60661-2511, and Northeast
Regional Office, 7 World Trade Center, Suite 1300, New York, NY 10048. Copies of
such material can also be obtained at prescribed rates by writing to the Public
Reference Section of the Commission at 450 Fifth Street, N.W., Washington, D.C.
20549. Such reports and other information filed with the Commission may also be
available at the Commission's site on the World Wide Web at http:www.sec.gov.
The Company's Common Stock is listed on the American Stock Exchange,
and copies of its reports, proxy statements and other information filed with the
Commission under the Exchange Act, and other information concerning the Company,
can be inspected at the American Stock Exchange.
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SUMMARY OF THE PROSPECTUS
This summary is qualified in its entirety by the more detailed
information and financial statements appearing elsewhere in the Prospectus.
THE COMPANY
NetMed, Inc., formerly known as Papnet of Ohio, Inc., is an Ohio
corporation engaged in the business of acquiring, developing and marketing
medical and health-related technologies. The Company's revenues are currently
derived principally from the marketing of the PAPNET(R) Testing System and
Service, which are proprietary products of Neuromedical Systems, Inc. ("NSI").
The Company is also currently engaged in the development of an oxygen
concentration device that it plans to manufacture and sell in the home
healthcare market.
The PAPNET(R) Testing System is a semi-automated cancer detection
system for the review of cell, tissue or body fluid specimens, including but not
limited to cervical cytology specimens. The PAPNET(R) Service permits
laboratories to submit slides containing such specimens ("Slides") to one of
NSI's central facilities for image processing employing NSI's patented neural
network technology. NSI returns the Slides and digital tape or CD-ROM containing
processed images for evaluation by NSI-trained cytotechnologists. See "Business
- - The PAPNET(R) Testing System."
The FDA approved the PAPNET(R) Testing System for commercial use in the
United States on November 8, 1995. Prior to that time, it was permitted to be
utilized in the United States on an investigational basis only, and NSI was
permitted to derive revenue with respect thereto only to recover certain of its
costs. Beginning January 1, 1996, the Company and NSI began the task of building
a sales force and familiarizing doctors and laboratories with the benefits of
the PAPNET(R) Testing System and Service. Beginning in September of 1996, NSI
began the commercial launch of the product with a national advertising campaign.
On December 5, 1996, the Company's shareholders approved an Agreement
and Plan of Merger (the "Merger Agreement") whereby Cytology Indiana, Inc.,
Indiana Cytology Review Company, ER Group, Inc., CCWP Partners, Inc., and
Carolina Cytology, Inc. (the "Predecessor Companies") were merged with and into
Papnet of Ohio, Inc. (the "Merger"). The Merger was effective on December 16,
1996, and the Company issued 4,849,988 common shares, without par value, in
exchange for the issued and outstanding shares of the Predecessor Companies.
Pursuant to the Merger Agreement, the Company changed its name to NetMed, Inc.,
and its common shares began trading on the American Stock Exchange on December
18, 1996 under the symbol "NMD". See "Business - The Merger."
As a result of the Merger, the Company has the marketing rights to the
PAPNET(R) Testing System and Service in Ohio, Kentucky, Missouri, Georgia, North
Carolina and the Consolidated Statistical Area of Chicago. The Company's
marketing rights are exclusive within these territories, subject to the right of
NSI to conduct marketing and sales activities therein. However, because the
royalties paid to the Company by NSI are based on revenues recognized by NSI
from activities (including any sales by NSI) in the licensed territories, NSI's
sales activities therein benefit the Company. See "Business - The NSI License."
While the Company's primary focus has been, and will continue to be,
exploiting its rights under the NSI license, the Company will also consider the
acquisition of other healthcare related technologies in the future. In February
1997 the Company entered an agreement with CeramPhysics, Inc. of Westerville,
Ohio ("Ceram"), pursuant to which the Company has the right to acquire control
of a newly-organized corporation holding a world-wide license to Ceram's
patented oxygen generation technology, which is exclusive as to all applications
except oxygen sensors and fuel cells. The Company is currently engaged in the
development of an oxygen concentration device based on this technology, which it
plans to sell in the home healthcare market.
The Company's principal offices are located at 6189 Memorial Drive,
Dublin, Ohio 43017, and its telephone number at that address is (614) 793-9356.
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THE OFFERING
The shares offered hereby (the "Shares") consist of up to 1,500,000
common shares, without par value (the "Common Stock") of the Company which are
issuable by the Company to certain persons ("Selling Shareholders") upon
conversion of the 6% Convertible Subordinated Debentures of the Company
("Debentures"), and upon exercise by the Selling Shareholders of certain
warrants to purchase Common Stock ("Warrants"). The number of shares registered
for sale by this Prospectus equals approximately 150% of the number of Shares
into which the Debentures are convertible on September 10, 1997, assuming the
Debentures were fully convertible on such date, plus the number of Shares
issuable upon exercise of the Warrants.
THE DEBENTURES AND WARRANTS
The Debentures are due August 13, 2000, bear interest at a rate of 6%
per annum, and are redeemable by the Company. The Company issued the Debentures
to the Selling Shareholders on August 13, 1997 pursuant to the terms of
Convertible Debenture Purchase Agreements with the Selling Shareholders (the
"Purchase Agreements"). The Debentures and any interest accrued thereon may be
converted into Shares at any time. However, no sales of Shares may be made prior
to November 11, 1997, and during the period from November 11, 1997 through May
10, 1998 (the 91st through 270th day after the closing) the maximum aggregate
number of Shares which can be sold is 500,000. After May 10, 1998 (the 270th day
after the closing), 100% of the Shares may be sold. The Company can prohibit
sales during the period from December 14, 1997 to February 1, 1998 (the
"Blackout Period"). The Debentures are convertible into shares of the Company's
Common Stock based on the "Conversion Price" at the time of conversion, which
varies based on the date when the Debentures are converted. For the period
through March 31, 1998, the Conversion Price is an amount equal to 80% of the
average closing bid price of the Common Stock on the American Stock Exchange for
the previous three business days ending on the day before the conversion date.
For the period beginning April 1, 1998, the Conversion Price is an amount equal
to 75% of the average closing bid price of the Common Stock on the American
Stock Exchange for the previous three business days ending on the day before the
conversion date. The Warrants are exercisable at any time prior to August 13,
2000 at exercise prices of $7.79 per Share (for up to 150,000 Shares) and $9.35
per Share (for up to 65,000 Shares).
The Debentures are secured by 475,000 shares of common stock of
Neuromedical Systems, Inc. (Nasdaq: NSIX) owned by the Company (the "NSI
Shares"). If at any time prior to March 31, 1998, the conversion price is $3.00
or less, the holders of the Debentures may elect to exercise their conversion
rights for NSI Shares, rather than Common Stock of the Company, at a 20%
discount from the market price at the time of conversion. If the Company
prohibits sales during the Blackout Period, and the trading volume in the Common
Stock prior to December 15, 1997 does not meet defined minimums, the holders may
convert into the NSI Shares at a discount from the market price which would
produce a 25% return on an annualized basis. The NSI Shares may be released from
the pledge ratably as the outstanding principal amount of Debentures is reduced.
For a further description of the terms of the Debentures and the
Warrants see "Selling Shareholders."
SHARES OUTSTANDING
Common Stock Outstanding .......... 10,947,114 shares
American Stock Exchange Symbol .... NMD
Use of Proceeds ................... The Company will not receive any
proceeds from the sale of Shares by
the Selling Shareholders.
RISK FACTORS
Before making an investment in the Common Stock, prospective purchasers
should carefully consider the factors set forth in this Prospectus under "Risk
Factors."
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RISK FACTORS
Investment in the securities being offered hereby involves a high
degree of risk, including, but not limited to, the risk factors described below.
Prospective investors should carefully consider the following risk factors, in
addition to the other information in this Prospectus, in evaluating an
investment in the securities offered hereby.
HISTORY OF LOSSES; PROFITABILITY UNCERTAIN; RELIANCE ON A SINGLE PRODUCT
The Company is in the early stage of its operations, and is therefore
subject to risks incident to any new business, including the absence of
earnings. The Company has to date had limited income from operations, and as of
June 30, 1997 has an accumulated deficit of $1,386,496. While the Company
intends to complete development and commercialization of its oxygen
concentration device, it has to date concentrated its efforts primarily on the
marketing of the PAPNET(R) Testing System and will be dependent for the
foreseeable future upon the successful marketing of that product to generate
revenues.
The Company cannot accurately predict the extent of its future capital
needs, but anticipates that expenditures will increase significantly during the
remainder of 1997 and through 1998 due to marketing costs for the PAPNET(R)
Testing System and completion of development and commercialization of the oxygen
concentrator. A significant amount of the Company's assets are represented by
its investment in NSI common stock, the liquidation of which will provide a
supplemental source of financing for the Company's activities. There can be no
assurance regarding the market value of the NSI common stock and any decrease in
its market value may adversely impact the Company's total assets and its ability
to fund its business plan. In addition, there can be no assurance that other
funds will be available on terms favorable to the Company, or at all. If
additional funds are raised through the issuance of equity securities, the
percentage ownership of the then current shareholders of the Company may be
reduced and such equity securities may have rights, preferences or privileges
senior to those of the holders of the Company's common shares. See "Business"
and "Management's Discussion and Analysis of Financial Condition and Results of
Operations."
DEPENDENCE ON NSI; NO OWNERSHIP OF PAPNET(R) TECHNOLOGY
The Company obtains all of the information relating to the PAPNET(R)
Testing System and Service from NSI, and in most cases cannot independently
verify this information. Therefore, the Company is dependent on NSI to
accurately report the results of clinical studies and other data relating to the
capabilities and performance of the PAPNET(R) Testing System.
The Company has no ownership rights in the PAPNET(R) technology. NSI
has granted the Company exclusive rights with respect to the marketing of the
PAPNET(R) Testing System and Service in certain geographic territories.
Therefore, the business of the Company is dependent upon a number of factors,
many of which are controlled by NSI. These factors include maintaining the
PAPNET(R) Testing System's compliance with FDA and other regulatory
requirements, maintenance of the technological advantages of the PAPNET(R)
Testing System, maintenance of product liability insurance, and the ability to
manufacture and deliver the equipment required to operate the PAPNET(R) Testing
System. Further, NSI is in a stage of development that may require additional
funding for its internal operations. In the event that NSI should fail to
perform in any of these areas, or in any others which could affect its
licensees, such failure could have an adverse effect on the Company and its
business. See "Business - NSI - Licensor of the PAPNET(R) System."
Additional risks relating to the business of NSI which may have an
impact on the Company are set forth in NSI's periodic reports filed with the
Commission, including its Annual Report on Form 10-K.
NSI LICENSE AGREEMENT AND PATENTS
The Company's marketing rights and the revenues generated by these
activities, are governed by the terms of its license from NSI (the "License").
The License imposes significant territorial and other restrictions on the
Company's marketing rights, and places certain limitations on the amounts of
royalty revenues which the Company can generate through the marketing of the
PAPNET(R) Testing System and Service. The terms of the License are set
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forth in the form of license agreement incorporated into the Settlement
Agreement, but to date the Company and NSI have not executed a definitive
license agreement. See "Business - The NSI License."
The technology underlying the PAPNET(R) Testing System is protected by
broad patent protection granted to NSI with respect to the use of neural
networks in automated and semi-automated cytology. There can be no assurance
that the NSI patents will afford protection from material infringement or that
such patents will not be challenged. NSI and the Company will also rely on trade
secrets and proprietary know-how, which they will seek to protect, in part,
through confidentiality agreements with employees, consultants and other
parties. There can be no assurance that these agreements will not be breached,
that there will be adequate remedies for any breach or that trade secrets of NSI
or the Company will not otherwise become known to, or independently developed
by, competitors.
The medical device industry has been characterized by extensive
litigation regarding patents and other intellectual property rights. Although
patent and intellectual property disputes in the medical device area have often
been settled through licensing or similar arrangements, costs associated with
such arrangements may be substantial and there can be no assurance that
necessary licenses would be available to NSI or the Company on satisfactory
terms or at all. Adverse determinations could limit the value of NSI's issued
patents or result in invalidation of those patents, subject NSI or the Company
to significant liabilities to third parties, require NSI or the Company to seek
licenses from third parties or prevent NSI from manufacturing its products or
prevent NSI or the Company from selling NSI's products, any of which could have
a material adverse effect on the Company's business, financial condition and
results of operations.
DEPENDENCE UPON KEY PERSONNEL
The success of the Company's operations is highly dependent upon David
J. Richards, its founder and President, as well as its other key executive
officers. The loss of any of these persons could have an materially adverse
effect on the Company. See "Management."
GOVERNMENT REGULATION
The services, products and manufacturing activities of NSI and the
Company are subject to extensive and rigorous government regulation, including
the provisions of the Medical Device Amendment to the Federal Food, Drug and
Cosmetic Act. Commercial distribution in certain foreign countries is also
subject to government regulations. The process of obtaining required regulatory
approvals can be lengthy, expensive and uncertain. Moreover, regulatory
approvals, if granted, may include significant limitations on the indicated uses
for which a product may be marketed. The FDA actively enforces regulations
prohibiting marketing without compliance with the premarket approval provisions
of products and conducts periodic inspections to determine compliance with Good
Manufacturing Practice regulations.
Failure to comply with applicable regulatory requirements can result in,
among other things, fines, suspensions of approvals, seizures or recalls of
products, operating restrictions and criminal prosecutions. Furthermore, changes
in existing regulations or adoption of new regulations could prevent NSI or the
Company from obtaining, or affect the timing of, future regulatory approvals.
The effect of governmental regulation may be to delay for a considerable period
of time or to prevent the marketing and/or full commercialization of future
products or services that NSI or the Company may develop and/or impose costly
requirements on NSI or the Company. There can be no assurance that NSI or the
Company will be able to obtain regulatory approvals of any products on a timely
basis or at all. Delays in receipt of or failure to receive such approvals or
loss of previously received approvals would adversely affect the marketing of
NSI's and the Company's proposed products. There can also be no assurance that
additional regulations will not be adopted or current regulations amended in
such a manner as will materially adversely effect NSI or the Company.
LIMITED THIRD PARTY REIMBURSEMENT
In the United States, many Pap smears are currently paid for by the
patient, and the level of reimbursement by third-party payers that do provide
reimbursement differ considerably. Third-party payers (Medicare/Medicaid,
private health insurance, health maintenance organizations, health
administration authorities in foreign countries and
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other organizations) may affect the pricing or relative attractiveness of the
Company's and NSI's products and services by regulating the maximum amount of
reimbursement for products or services provided by the Company and NSI or by not
providing any reimbursement at all. Restrictions on reimbursement may limit the
price which the Company can charge for its products and services or reduce the
demand for them, or, in the case of PAPNET(R) testing, if the level of such
reimbursement is significantly below what laboratories charge patients to
perform the test, the size of the potential market available to the Company may
be reduced. There can be no assurance of the extent to which costs of PAPNET(R)
testing will become reimbursable or that the level of reimbursement will be
sufficient to permit the Company to generate substantial revenues. See "Business
- - Third Party Reimbursement."
MARKETABILITY AND COMPETITION
The Company's future performance will depend to a substantial degree
upon market acceptance of the PAPNET(R) Testing System. The extent of, and rate
at which, market acceptance and penetration are achieved are functions of many
variables including, but not limited to, price, effectiveness, acceptance by
patients, physicians and laboratories (including the ability of laboratories to
hire additional cytotechnologists), manufacturing, slide processing and training
capacity, reimbursement practice and marketing and sales efforts. There can be
no assurance that the PAPNET(R) Testing System will achieve or maintain
acceptance in its target markets.
The Company is aware of several companies that either have developed or
are developing systems that are competitive with the PAPNET(R) Testing System or
other technologies targeted for development by the Company. Commercial
availability of such products could have a material adverse effect on the
Company's business, financial condition and results of operations. Competitors
may have substantially greater financial, manufacturing, marketing and technical
resources, and represent significant potential long-term competition.
Competitors may succeed in developing products that are more effective or less
costly than any that may be developed by NSI or the Company. New developments
are expected to continue at a rapid pace in both industry and academia. There
can be no assurance that research and development by others will not render
NSI's or the Company's current and contemplated products obsolete. Competition
may increase further as a result of advances that may be made in the commercial
applicability of technologies and greater availability of capital for investment
in these fields. See "Business - Competition in the Cervical Cytology Market."
PRODUCT LIABILITY
The business of the Company could expose it to the risks inherent in the
production and distribution of medical diagnostic and treatment equipment.
Although NSI has attempted to reduce the exposure to product liability risk by
disclosing the demonstrated range of accuracy of the PAPNET(R) Testing System,
there can be no assurance that the Company will not be exposed to liability
resulting from the failure or inaccuracy of the PAPNET(R) System. The Company
currently carries no product liability insurance. However, NSI is required,
under the terms of the License, to name the Company as an additional insured on
its product liability policies. There can be no assurance that NSI will have the
resources necessary to purchase and maintain the insurance, that such insurance
will be sufficient to cover potential claims, or that NSI will have adequate
resources to indemnify the Company from any uninsured loss.
DIVIDEND POLICY
The Company does not contemplate the payment of dividends for the
foreseeable future. The Company has accumulated substantial losses since its
inception and there can be no assurance that the Company's operations will
result in sufficient revenues to enable the Company to operate at profitable
levels or to generate positive cash flow. Any earnings generated from the
operations of the Company will be used to finance the business and growth of the
Company. See "Price Range of Common Stock and Dividend Policy."
CONTROL BY AFFILIATES
The directors, executive officers and principal shareholders (5% or
greater) of the Company collectively own approximately 30% of the outstanding
Common Stock. As a result, these shareholders will be able to exercise
significant influence over matters requiring shareholder approval, including the
election of directors and approval of significant corporate transactions. Such
concentration of ownership may have the effect of delaying or preventing a
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change in control of the Company. See "Ownership of Common Stock by Management
and Principal Shareholders."
SHARES ELIGIBLE FOR FUTURE SALE
The Company had 10,947,114 common shares outstanding as of August 31,
1997. Approximately 2,650,000 shares are held by affiliates of the Company who
will be entitled to resell them only pursuant to a registration statement under
the Securities Act or an applicable exemption from registration thereunder such
as provided by Rule 144 under the Securities Act. Approximately an additional
3,637,000 are currently subject to certain restrictions on transfer as a result
of the Merger, all of which will expire on December 16, 1997, whereupon such
shares will become freely tradable without any restriction.
Sales of substantial amounts of the Company's shares in the public
market or the prospect of such sales could adversely affect the market price of
its shares.
LIQUIDITY; POSSIBLE VOLATILITY OF STOCK PRICE
Although the Common Stock is currently listed for trading on the
American Stock Exchange, trading volume has been limited. There can be no
assurance that there will continue to be an active and liquid trading market.
The stock market has experienced extreme price and volume fluctuations and
volatility that has particularly affected the market prices of many technology,
emerging growth and developmental stage companies. Such fluctuations and
volatility have often been unrelated or disproportionate to the operating
performance of such companies. Factors such as announcements of the introduction
of new or enhanced services or related products by the Company or its
competitors may have a significant impact on the market price of the Common
Stock. Sales by the Selling Shareholders of the Shares which are the subject of
this Prospectus may also adversely affect the pricing and volatility of trading
in the Common Stock. See "Price Range of Common Stock and Dividend Policy."
Market prices of securities of medical technology companies, including
the Common Stock, have experienced significant volatility from time to time.
There may be volatility in the market price of the Common Stock due to factors
that may or may not relate to the Company's performance. Various factors and
events, such as announcements by the Company or its competitors concerning new
product developments, governmental approvals, regulations or actions,
developments or disputes relating to patent or proprietary rights and public
concern over product liability may have a significant impact on the market price
of the Common Stock.
PRICE RANGE OF COMMON STOCK AND DIVIDEND POLICY
Since the completion of the Merger, the Common Stock has been listed on
the American Stock Exchange and trades under the symbol "NMD."
The Common Stock is listed for trading on the American Stock Exchange
under the symbol "NMD." Prior to December 18, 1996, the Company's Common Shares
were traded in the over the counter market on the NASDAQ Bulletin Board. The
following table sets forth, for the periods indicated, the high and low last
sales prices per share, as reported on the NASDAQ Bulletin Board, and
subsequently on the American Stock Exchange. The figures have been adjusted to
reflect 2-for-1 stock splits in May and December 1995. The prices shown through
December 17, 1996 represent inter-dealer prices, without adjustments for retail
markups, markdowns or commissions and may not represent actual transactions.
First Quarter 1995 ........... $ 5.398 $ 3.75
Second Quarter 1995 .......... 8.094 7.875
Third Quarter 1995 ........... 17.688 10.75
Fourth Quarter 1995 .......... 15.688 13.375
First Quarter 1996 ........... 13.00 9.375
Second Quarter 1996 .......... 10.75 8.375
Third Quarter 1996 ........... 9.00 7.125
Fourth Quarter 1996 .......... 8.875 6.25
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First Quarter 1997 ........... 9.625 6.625
Second Quarter 1997 .......... 7.875 5.00
On September __, 1997, the last reported sale price of the Common Stock
was $___ per share. On September __, 1997, there were ____ holders of record of
the Common Stock.
The Company has not paid and does not anticipate paying any cash
dividends in the foreseeable future and intends to retain future earnings for
the development and expansion of its business. Any future determination to pay
dividends will be at the discretion of the Board and subject to certain
limitations under the Ohio General Corporation Law and will depend upon the
Company's results of operations, financial condition, contractual restrictions
and other factors deemed relevant by the Board.
USE OF PROCEEDS
The Company will not receive any proceeds from the sale of the Shares
by the Selling Shareholders.
SELECTED FINANCIAL DATA
The following selected financial data of the Company are qualified by
reference to and should be read in conjunction with "Management's Discussion and
Analysis of Financial Condition and Results of Operations" and the financial
statements and notes thereto included elsewhere in this Prospectus. The selected
financial data for the years ended December 31, 1993, 1994, 1995 and 1996 are
derived from the Company's audited financial statements for those years. The
selected financial data for the year ended December 31, 1992 and for the
six-month periods ended June 30, 1996 and 1997 are derived from unaudited
financial statements of the Company. The unaudited financial statements included
elsewhere in this Prospectus and, in the opinion of the Company, include all
adjustments, consisting of normal recurring accruals considered necessary for a
fair and consistent presentation of such information.
Year ended December 31, Six Months Ended June 30,
----------------------- -------------------------
1992 1993 1994 1995 1996 1997 1996
---- ---- ---- ---- ---- ---- ----
Revenue $ 27,989 $ 4,322 $ 24,765 $ 48,000 $ 102,813 $ 339,608 $ 27,099
Loss from operations (210,148) (285,591) (302,596) (525,149) (1,677,312) (1,210,046) (364,358)
Net income (loss) (202,702) (277,068) (283,537) 1,324,945 (592,822) (585,194) (235,577)
Net Income (loss) per share - - (0.05) 0.21 (0.09) (0.05) (0.04)
BALANCE SHEET DATA:
Total assets 833,074 962,492 768,934 9,225,744 10,379,590 4,403,611 6,724,648
Total Stockholders' equity 412,257 923,828 738,600 6,253,679 7,035,067 3,179,293 4,778,179
MANAGEMENT'S DISCUSSION AND ANALYSIS OF
FINANCIAL CONDITION AND RESULTS OF OPERATIONS
OVERVIEW
The Company is an Ohio corporation engaged in the business of
acquiring, developing and marketing medical and health-related technologies. The
Company's revenues are currently derived principally from the marketing of the
PAPNET(R) Testing System and Service, which are proprietary products of NSI. The
Company is also currently engaged in the development of an oxygen concentration
device which it plans to manufacture and sell in the home healthcare market.
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The PAPNET(R) Testing System is a semi-automated cancer detection
system for the review of cell, tissue or body fluid specimens, including but not
limited to cervical cytology specimens. The PAPNET(R) Service permits
laboratories to submit slides containing such specimens to one of NSI's central
facilities for image processing employing NSI's patented neural network
technology. NSI returns the Slides and digital tape or CD-ROM containing
processed images for evaluation by NSI-trained cytotechnologists.
The PAPNET(R) Testing System was approved by the FDA for commercial use
in the United States on November 8, 1995. Prior to that time, it was permitted
to be utilized in the United States on an investigational basis only, and NSI
was permitted to derive revenue with respect thereto only to recover certain of
its costs. Beginning January 1, 1996, the Company and NSI began the task of
building a sales force and familiarizing doctors and laboratories with the
benefits of the PAPNET(R) Testing System and service. Beginning in September of
1996, the commercial launch of the product was initiated with a national
advertising campaign.
On December 5, 1996, the Company's shareholders approved the Merger
with the Predecessor Companies. The Merger was effective on December 16, 1996,
and the Company issued 4,849,988 common shares, without par value, in exchange
for the issued and outstanding shares of the Predecessor Companies. Pursuant to
the Merger Agreement, the Company changed its name to NetMed, Inc., and its
common shares began trading on the American Stock Exchange on December 18, 1996
under the symbol "NMD".
As a result of the Merger, the Company has the marketing rights to the
PAPNET(R) Testing System and Service in Ohio, Kentucky, Missouri, Georgia, North
Carolina and the Consolidated Statistical Area of Chicago. The Company's
marketing rights are exclusive within these territories, subject to the right of
NSI to conduct marketing and sales activities therein. However, because the
royalties paid to the Company by NSI are based on revenues recognized by NSI
from activities (including any sales by NSI) in the licensed territories, NSI's
sales activities therein benefit the Company.
While the Company's primary focus has been, and will continue to be,
exploiting its rights under the NSI license, the Company will also consider the
acquisition of other healthcare related technologies in the future. In February,
1997 the Company announced that it had entered an agreement with CeramPhysics,
Inc. of Westerville, Ohio, pursuant to which the Company has the right to
acquire control of a newly-organized corporation holding a world-wide license to
Ceram's patented oxygen generation technology, which is exclusive as to all
applications except oxygen sensors and fuel cells.
For accounting purposes, the financial statements of the Company for
1996 and prior years are those of Papnet of Ohio, Inc. The results of operations
for the merged entities are reported on a prospective basis commencing December
16, 1996. The following discussion therefore includes the operations of Papnet
of Ohio, Inc. from January 1, 1996 through June 30, 1996, and the consolidated
operations of all entities from January 1, 1997 through June 30, 1997.
RESULTS OF OPERATIONS
For the Six Months ended June 30, 1997 and 1996
As a result of the FDA approval mentioned above, the commercial launch
of the product in September 1996 and an increase in the number of sales
representatives, the number of Slides processed in the Company's territories
increased to 41,302 Slides for the six months ended June 30, 1997 from 4,216
Slides for the six months ended June 30, 1996. On a proforma basis, 6,469 Slides
were processed for the Company and the Predecessor Companies for the six months
ended June 30, 1996. Royalty revenue was $339,608 for the six months ended June
30, 1997, an increase from $27,099 for the six months ended June 30, 1996.
In February 1997, the Company entered into an agreement with Blue Cross
Blue Shield Mutual of Ohio, now known as Medical Mutual of Ohio ("MMO"), whereby
MMO agreed to cover the cost of the PAPNET(R) test for all members. In addition,
MMO has agreed to strongly recommend to its clinicians and laboratories that all
negative Pap smears covered by its benefit plans be examined using PAPNET(R)
testing. MMO is one of the largest third party payers for health care in the
State of Ohio, with approximately 1.5 million covered members. While management
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believes that this agreement will eventually increase the number of Slides
processed during 1997, the Company is unable to quantify the impact of the
agreement on Slide volume for the six months ended June 30, 1997, although it
believes such impact was minimal.
The number of employees of the Company increased to 15 during the six
months ended June 30, 1997, an increase of 10 employees from the same period the
previous year. The increase consisted of an additional six sales representatives
and four administrative employees. As a result of granting options to certain
employees and directors during the six months ended June 30, 1997, the Company
incurred compensation expense of $131,275. This amount has been included in
salaries and benefits. As a result of the headcount increases mentioned above
and the expense for the grant of options, salary and benefit expense increased
to $762,557 for the six months ended June 30, 1997 from $146,733 for the six
months ended June 30, 1996.
Sales and marketing expense other than salaries and benefits increased
to $376,657 for the six months ended June 30, 1997 from $52,533 for the six
months ended June 30, 1996. In addition to the direct expenses of the sales
representatives in developing their respective sales territories, the Company
incurred expenses for advertising, promotional materials and sales literature of
$183,182. The Company incurred a total of $47,500 for professional services in
its efforts to expand the reimbursement of the cost of the PAPNET(R) test by
healthcare providers and for employment agency fees for the additional sales
representatives hired during the six months ended June 30, 1997.
General and administrative expenses increased to $351,095 for the six
months ended June 30, 1997 compared to $57,741 for the six months ended June 30,
1996. The increase in general and administrative expense is primarily due to an
increase in accounting, legal and stock exchange costs as well as the increase
in headcount from two to six administrative employees.
Consistent with the Company's plan to acquire compatible business
technologies, the Company incurred costs of $59,345 for the six months ended
June 30, 1997 in the negotiation and evaluation of additional opportunities in
medical technology. In February 1997, the Company announced that it had entered
an agreement with CeramPhysics, Inc. of Westerville, Ohio, pursuant to which the
Company has the right to acquire control of a newly-organized corporation
holding a world-wide license to Ceram's patented oxygen generation technology,
which is exclusive as to all applications except oxygen sensors and fuel cells.
During 1995, the Company began discussions with the Predecessor
Companies that resulted in the Merger that was effective December 16, 1996. For
the six months ended June 30, 1996, the Company incurred one time merger
expenses of $134,450. No expenses related to this transaction were incurred in
the six months ended June 30, 1997.
The Company recognized a gain on available-for-sale securities of
$745,056 for the six months ended June 30, 1997. There were no sales of
securities during the six months ended June 30, 1996. The increase is due to the
gain on the sale of 125,000 shares of NSI common stock held by the Company at
net prices ranging from $5.07 to $10.13 per share.
Interest income for the six months ended June 30, 1997 was $2,099
compared to $10,871 for the same period the prior year. The decrease was a
result of lower available cash balances to invest, as cash balances have been
utilized to fund the negative cash flow from operations.
The Company incurred loans payable of $140,913 as of June 30, 1997. The
loans are the result of opening margin accounts utilizing NSI common stock for
collateral. Interest expense as a result of these loans was $4,884 for the six
months ended June 30, 1997.
The Company recognized income tax expense of $117,419 for the six
months ended June 30, 1997, compared to an income tax benefit of $122,001 for
the six months ended June 30, 1996. The expense for the first half of 1997 is
the result of recording a valuation allowance against the deferred tax asset of
$288,000. The deferred tax liability was reduced during the period as a result
of the decline in market value of the NSI common stock. Since the deferred tax
liability is subject to the fluctuations in market price of the NSI common
stock, the Company may recognize additional expense or benefit in future
periods.
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The equity in income or loss in partnerships reported for the six
months ended June 30, 1996 is the Company's percentage of income or loss in
Carolina Cytology Licensing Company and Carolina Cytology Warrant Partnership.
Both entities were Predecessor Companies and were merged into the Company on the
effective date of the Merger, and consequently no similar item is reported for
the same period in 1997.
For the Years Ended December 31, 1994, 1995 and 1996
The PAPNET(R) Testing System was approved by the FDA for commercial use
in the United States on November 8, 1995. Prior to that time, it was permitted
to be utilized in the United States on an investigational basis only, and NSI
was permitted to derive revenue with respect thereto only to recover certain of
its costs. Therefore, the Company was able to generate only a minimal amount of
revenue from the PAPNET(R) Testing System during 1994 and 1995. During the first
eight months of 1996, the Company and NSI spent time and effort building a sales
force and familiarizing doctors and laboratories with the benefits of the
PAPNET(R) Testing System and Service. Beginning in September of 1996, the
commercial launch of the product was initiated with a national advertising
campaign.
As a result of the FDA approval mentioned above and the commercial
launch of the product in September 1996, the number of Slides processed
increased to 13,820 Slides for the year ended December 31, 1996 from 1,529
Slides for the year ended December 31, 1995. There were no Slides processed
during 1994. Royalty revenue was $102,813, $48,000 and $24,765 for the years
ended December 31, 1996, 1995 and 1994, respectively.
Revenue for the year ended December 31, 1996 has been accrued according
to a formula in the Company's license agreement with NSI which calculates
royalties based upon the number of Slides processed in the Company's territory.
Revenue for the years ended December 31, 1995 and 1994 was accrued using an
alternative royalty formula based upon a percentage of NSI's worldwide revenue.
In anticipation of FDA approval for the PAPNET(R) test, the Company
began hiring additional sales representatives beginning in the third quarter of
1995 bringing the total to three by December 31, 1995 from one at December 31,
1994. At December 31, 1996 the Company employed a total of six sales
representatives. An additional two sales representatives and a Sales Director
were hired during the first quarter of 1997. In addition, the Company increased
the administrative staff from two during 1994 and 1995 to a total of five by
December 31, 1996. As a result of the headcount increases mentioned above,
salary and benefit expense increased to $441,762 for the year ended December 31,
1996 from $303,105 and $196,825 for the years ended December 31, 1995 and 1994
respectively.
While the Company had incurred costs to market and promote the
PAPNET(R) Testing System in the years ended December 31, 1994 and 1995, the
amount of expenditure increased significantly during 1996. Sales and marketing
expense other than salaries and benefits was $250,389 for the year ended
December 31, 1996 an increase from $74,329 and $26,433 for the years ended
December 31, 1995 and 1994, respectively. In addition to the direct expenses of
the sales representatives in developing their respective sales territories, the
Company incurred additional expenses for advertising, promotional materials and
sales literature. The Company incurred expense of $80,000 for professional
services in its efforts to expand the reimbursement of the cost of the PAPNET(R)
test by healthcare providers for the year ended December 31, 1996.
General and administrative expenses increased to $240,562 for the year
ended December 31, 1996 compared to $89,299 and $104,103 for the years ended
December 31, 1995 and 1994, respectively. The Company incurred one time costs
for registering with the American Stock Exchange and state securities fees
associated with increasing the number of authorized shares of the Company of
approximately $74,000 for the year ended December 31, 1996. In addition, general
and administrative expense increased due to the increase in headcount as well as
the cost of additional office space beginning in the fourth quarter of 1996.
During 1995, the Company began discussions with the Predecessor
Companies that resulted in the Merger that was effective December 16, 1996. For
the year ended December 31, 1996, the Company incurred one time merger expenses
of $364,852 compared to $106,415 in the year ended December 31, 1995.
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While the Company's primary focus has been, and will continue to be,
exploiting its rights under the NSI license, the Company will also consider the
acquisition of compatible business technologies in the future. Consistent with
that plan, the Company incurred costs of $85,476 for the year ended December 31,
1996 in the negotiation and evaluation of additional opportunities in medical
technology.
On December 5, 1995 the Company and the Predecessor Companies entered
into a Settlement Agreement with NSI (the "Settlement Agreement"). The purpose
of the Settlement Agreement was to resolve and clarify certain issues relating
to the license agreements which NSI had with its regional licensees, and issues
relating to warrants to purchase shares of NSI common stock which were held by
the Company and certain of the Predecessor Companies. As a result of exercising
NSI warrants, settling claims with NSI and buying and selling NSI stock from
NSI's initial public offering, the Company recorded other income of $1,715,399
in the year ended December 31, 1995. The Company has reported a gain on the sale
of securities available-for-sale of $664,057 in the year ended December 31,1996
which has been recorded as other income.
The equity in income or loss in partnerships is the Company's
percentage of income or loss in Carolina Cytology Licensing Company and Carolina
Cytology Warrant Partnership. Both entities were Predecessor Companies and were
merged into the Company on the effective date of the Merger.
LIQUIDITY AND CAPITAL RESOURCES
The Company has financed its operations to date primarily by the sale
of NSI common stock owned by the Company, the sale of Common Stock, and the sale
of the Debentures. Including the net proceeds of the sale of the Debentures in
August 1997 of $2,805,000, the Company's combined cash and cash equivalents
totaled $2,525,000 at August 31, 1997, an increase of $2,383,000 from December
31, 1996. The Company owns 572,246 unrestricted shares of NSI common stock which
can be liquidated in an orderly fashion to fund future operations. NSI common
stock closed trading at $3.50 per share on August 31, 1997.
While the Company anticipates that its cash requirements will be
substantial for the immediate future, it believes its existing investments will
be adequate to meet those requirements. The cash requirements relate
specifically to the accounts and loan payable and accrued expenses at August 31,
1997 of approximately $300,000, the continuing negative cash flow generated from
operations on a monthly basis and the costs associated with the sales and
marketing efforts to healthcare providers, doctors, laboratories and direct to
the consumer during 1997 and potentially 1998. The sales and marketing expenses
include, but are not limited to, the cost of expanding the sales force, direct
advertising to consumers, advertising and promotion expense associated with the
implementation of the MMO contract and professional fees associated with
marketing to healthcare providers. The professional fees associated with
marketing to healthcare providers are necessary as the current sales force is
responsible for marketing primarily to doctors and laboratories. While
management believes that the above strategies will increase Slide volume, there
can be no guarantee as to the timing and the amount of increase, if any.
In addition to exploiting its rights under the license agreement with
NSI, the corporate mission of the Company is to become a well diversified health
care technology company founded upon proprietary products that offer a distinct
market advantage. The Company's intention is to follow the example of the
initial investment, the PAPNET(R) technology, in pursuing other opportunities in
healthcare technology. Specifically, the Company intends to make early
investments and applying the management and marketing resources of the Company
to develop and implement strategies which will substantially increase the value
of the investment over a period of two to four years. As opportunities become
available, the Company will require substantial funds in making the initial
investment and/or commercializing new healthcare products.
In pursuit of that strategy, the Company has recently embarked upon the
development of an oxygen generation/concentration device for use in home
healthcare, based upon technology acquired from Ceram. Pursuant to the
agreement, the Company will work with and loan up to $200,000 to Ceram to
complete the fabrication and testing of a ceramic element incorporating the
licensed technology, which will be capable of generating oxygen of a purity and
in quantities suitable for medical use. As of August 31, 1997, advances to Ceram
have totaled $151,510. It is the Company's intention to incorporate the element
into an oxygen generation device which the Company will manufacture and market
for the home health care market. If the device is acceptable to the Company, it
has the right
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to acquire 95% of the capital stock of the licensee for an additional $200,000
investment, with the remaining 5% to be held by Ceram.
Thereafter, the Company would complete the development of a commercial
version of the device, proceed with obtaining appropriate regulatory approvals,
and commence manufacturing, marketing and distribution of the product. Such
activities are likely to require substantial expenditures in late 1997 and
during 1998, and depending upon the ultimate methods of manufacture, marketing
and distribution chosen by the Company, may require it to seek additional
capital in 1998.
BUSINESS
GENERAL
The Company is an Ohio corporation engaged in the business of
acquiring, developing and marketing medical and health-related technologies. The
principal business activity of the Company is the marketing of the PAPNET(R)
Testing System, which is a proprietary product of NSI. The PAPNET(R) Testing
System is a semi-automated cancer detection system for the review of cell,
tissue or body fluid specimens, including but not limited to, cervical cytology
specimens. Clinical laboratories submit slides containing cytology specimens to
one of NSI's central facilities for image processing using the PAPNET(R) Testing
System, which produces processed images for evaluation by NSI-trained
cytotechnologists.
The Company was originally organized in 1989 for the purpose of
acquiring the exclusive territorial rights to market NSI's proprietary products.
The Company organized two limited partnerships for this purpose, one of which
acquired the marketing rights in the State of Ohio, and the other which acquired
territorial rights for Kentucky and the Chicago, Illinois metropolitan area. In
1993 the Company acquired all of the issued and outstanding limited partnership
interests in both partnerships and thereby acquired all of the rights to market
the PAPNET(R) Testing System in Ohio, Kentucky and the Chicago metropolitan
area.
On December 16, 1996, the Company completed the Merger with the
Predecessor Companies, which had held the rights to market the PAPNET(R) Testing
System and Service in the states of Missouri, Georgia and North Carolina. The
Company was the surviving corporation in the Merger. Upon completion of the
Merger, the Company changed its name from Papnet of Ohio, Inc. to NetMed, Inc.
In addition to exploiting its rights under the license agreement with
NSI, the corporate mission of NetMed is to become a well diversified health care
technology company founded upon proprietary products that offer a distinct
market advantage. The Company's intention is to follow the example of its
initial investment, the PAPNET(R) technology, in pursuing other opportunities in
healthcare technology. Specifically, it intends to make early investments in
selected healthcare technologies and apply the management and marketing
resources of the Company to develop and implement strategies designed to
significantly increase the value of the investment over a period of two to four
years.
NSI - LICENSOR OF THE PAPNET(R) TESTING SYSTEM
NSI, founded in 1988, is a healthcare technology company focused on
diagnostic screening applications to aid in the early detection of certain
cancers. NSI's first product, the PAPNET(R) Testing System, is a supplemental
test to aid laboratories in the detection of abnormal cells on cervical
Papanicolaou ("Pap") smears which were not detected by the standard manual
microscopic inspection. When used to supplement manual screening of Pap smears,
PAPNET(R) testing has been shown to increase the detection of cervical
abnormality by up to 30% when compared to manual screening. The Company believes
that this improved detection can result in more effective and less costly early
treatment, reduced possibility of morbidity and mortality for patients, and
reduced possibility of malpractice litigation for the patient's doctor and
laboratory. The PAPNET(R) Testing System can achieve these improvements without
requiring a modification of the standard Pap smear sample due to its use of a
patented combination of algorithmic and adaptive pattern recognition technology,
a form of artificial intelligence.
The PAPNET(R) Testing System was approved for commercial use in the
United States by FDA on November 8, 1995. Thereafter, NSI commenced marketing to
laboratories and clinicians, and as of December 31,
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1996, the Papnet(R) test was available through 201 laboratories in the United
States, and was available in 23 countries worldwide. The PAPNET(R) Testing
System is a medical device subject to extensive regulation in the United States
by the FDA and other federal, state and local authorities. The FDA regulates the
research, development, clinical studies, manufacturing, processing, packaging,
labeling, distribution, promotion and post-market surveillance of medical
devices in the United States. The Company relies entirely upon NSI to assure
that all of these activities, as they relate to the PAPNET(R) Testing System,
comply with all applicable regulatory requirements.
THE CERVICAL CYTOLOGY MARKET
Pap smears are widely used in North America, Europe and other developed
areas to aid in the early detection of cervical cancer with over 50 million
tests performed annually in the U.S. alone. Pap smears can reveal early changes
in cervical cells that precede or indicate the development of cancer, thereby
facilitating timely medical intervention. When cervical cancer or precancerous
conditions are detected early on a Pap smear, the disease is almost always
completely curable using a simple outpatient procedure. However, if abnormal
cells on the Pap smear are not noticed by the laboratory, the patient may be
falsely told that her Pap smear is negative (a "false negative"), with
significant morbidity or mortality occurring as a result. Failure to diagnose
cervical cancer is a significant and rapidly growing source of malpractice
litigation against laboratories and clinicians in both the U.S. and abroad.
Manual searching of routine Pap smears to spot abnormal cells is an
unavoidably tedious and error-prone task. This is primarily because a seriously
abnormal Pap smear can contain fewer than a dozen abnormal cells scattered among
hundreds of thousands of normal cells and other objects. The cytotechnologist's
job is thus very similar to proofreading a very long document to try to detect a
few misspelled words. Regardless of how conscientious and careful the laboratory
is, many of these "needles in a haystack" may be missed, and the patient falsely
informed that her Pap smear was negative. Manual screening false-negative rates
ranging from 10% to 40% have been reported in numerous published studies. The
PAPNET(R) Testing System has been shown in several domestic and international
clinical studies published in peer-reviewed journals to detect abnormal cells on
Pap smears that were falsely diagnosed as "negative" by conventional manual
inspection. Indeed, in a number of such cases the PAPNET(R) Testing System
detected abnormal cells on archived, supposedly "negative" Pap smears of women
who were ultimately diagnosed with advanced cervical cancer. A published review
of six such studies which in the aggregate evaluated 513 Pap smears known to
contain precancerous or cancerous abnormality reported a pooled average
PAPNET(R) false negative rate of 3%. These results compare extremely favorably
to manual screening's false negative rate, typically reported to be many times
higher (10% to 40%).
THE PAPNET(R) TESTING SYSTEM
The PAPNET(R) Testing System is a computerized image processing
service provided to laboratories. The laboratory performs PAPNET(R) testing when
specifically requested by clinicians, patients or third-party payers who wish to
minimize the probability of false negatives and their attendant medical and
legal consequences. Slides first diagnosed by a laboratory as "negative" using
manual inspection are sent to designated NSI facilities ("Scanning Centers") for
imaging on a PAPNET(R) Scanning Station, which is designed to inspect the
hundreds of thousands of cells and other objects on the slide. The PAPNET(R)
Scanning Stations' proprietary neural network computers are designed to select
color images of 128 potentially abnormal cells and cell clusters from each slide
for detailed video review (whether or not they are, in fact, abnormal). These
128 images from each slide are recorded on a digital tape cassette or CD-ROM
which is returned to the client laboratory within two to four working days along
with the referred Pap smear slides.
At the laboratory, a certified cytotechnologist specially trained in
the use of the PAPNET(R) Testing System evaluates the 128 color images from each
slide on the PAPNET(R) Review Station. The PAPNET(R) Review Station's software
ensures that the cytotechnologist displays each image at 200x magnification
(twice normal screening power) and permits the user to expand any image to 400x
magnification. If all of the images appear normal, the cytotechnologist
classifies the slide as "negative," and no further examination is required. NSI
has found that cytotechnologists experienced in the use of the PAPNET(R) Review
Station can review negative cases in substantially less time than it takes to
perform a conventional manual re-examination.
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If any one of the 128 images appears to the cytotechnologist to be
abnormal, the cytotechnologist classifies the slide as "review." The
cytotechnologist then refers to the "x, y" coordinates provided with each
PAPNET(R) image and uses the coordinates as a reference point to re-examine the
slide directly through the microscope. If, after direct inspection, the
cytotechnologist continues to believe that the slide contains abnormal cells, he
or she refers the slide to the laboratory's pathologist for a final diagnosis.
In no case does NSI, the Company, nor the PAPNET(R) Testing System make a
diagnosis of a slide or smear.
The PAPNET(R) Testing System is used as a supplement to current
practice and does not alter the clinician's procedure for the taking of smears
or the laboratory's method of staining or applying the coverslip. It provides an
additional and complementary level of screening for the purpose of decreasing
false negative Pap smear diagnoses.
COMPETITION IN THE CERVICAL CYTOLOGY MARKET
The Company is currently aware of three principal competitors which are
engaged in efforts to automate one or more aspects of cervical smear screening.
Two competitors, Cytyc and Autocyte, have focused on the development of devices
for the production, and, in the case of Autocyte, automated analysis, of
monolayer slides, a potential alternative to the conventional Pap smear method
of specimen collection and preparation. Cytyc received approval from the FDA in
May 1996 to market its ThinPrep(R) preparation to laboratories, for the purpose
of filtering out blood, mucus and other material from Pap smears. Autocyte has
submitted an application to the FDA for premarketing approval of its method, but
to date has not received FDA approval. With monolayer techniques, clinicians are
required to prepare special slides, and only a fraction of the cells and
background information displayed on the conventional slide is retained for
analysis. Because the PAPNET(R) Testing System uses the well-established method
of sample collection, it does not require clinicians to deviate from standard
practice in the preparation or visual screening of Pap smears. In July 1997,
several persons (including Carl Genberg, a shareholder of the Company and a
director of NSI) filed a citizen's petition with the FDA requesting that the FDA
reexamine its earlier approval of the ThinPrep(R) technology as a replacement
for the conventional Pap smear.
The other competitor, NeoPath, has received FDA approval for the use of
its AutoPap(R) System as part of a laboratory's quality control procedure.
According to NeoPath, the AutoPap(R) System is designed to sort purportedly
"negative" Pap smear slides into two groups, one classified as "negative" and
one classified for "review." The group of slides classified for review, which
constitutes a specified percentage of the whole, is again reviewed manually by
the cytotechnologist through a conventional microscope. NeoPath has stated that
it is developing a device for the fully automated primary screening (as opposed
to rescreening) of conventional Pap smears, and has submitted to the FDA a
pre-market approval supplemental application. On September 27, 1996, an FDA
Advisory Panel recommended that the FDA not approve the supplemental
application, pending completion of additional studies. NeoPath recently
announced that it has submitted an amendment to its supplemental application to
incorporate the results of such studies. NSI is currently engaged in litigation
with NeoPath alleging patent infringement, unfair competition and other tortious
conduct concerning the development and marketing of the AutoPap(R) System.
NeoPath has denied these allegations and has asserted counterclaims to the
effect that NSI has made false and misleading representations concerning the
AutoPap(R) System. NSI has stated that it believes NeoPath's assertions are
without merit.
These or other competitors may develop new products and technologies
that prove to be more effective than the PAPNET(R) Testing System or that may be
viewed by clinical laboratories as reducing operating costs (for example, by
reducing the number of cytotechnologists used in screening). In addition,
competitive products and technologies may be manufactured and marketed more
successfully than the PAPNET(R) Testing System. Such developments could render
the PAPNET(R) Testing System less competitive or possibly obsolete, and could
have a material adverse effect on NSI and the Company. NSI and the Company will
be required to compete with respect to product effectiveness, price,
manufacturing and slide processing efficiency, marketing capabilities and
customer service and support, areas in which they currently have limited
experience.
In addition to competitors attempting to develop fully automated or
semi-automated systems for the screening or rescreening of cervical samples,
there may in the future be alternate techniques or technologies for the
detection or prevention of cervical cancer. Although no such technique has been
demonstrated to be useful as a substitute for the Pap smear, there can be no
assurance that new techniques or technologies will not one day supplant or
replace the Pap smear in medical practice.
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POTENTIAL FUTURE NSI PRODUCTS
NSI has stated the belief that its technology can be adapted for use in
the early detection of cancers occurring at body sites in addition to the
uterine cervix, including the bladder, breast, esophagus, lung, oral cavity and
thyroid. Not all such cancers are commonly the subject of cytological analysis,
and NSI has not yet determined which of these applications, if any, it will be
able to commercialize. However, NSI has announced that a study reported at a
recent meeting of the U.S. and Canadian Academy of Pathology showed that the
PAPNET(R) Testing System could detect cancerous and precancerous cells of the
esophagus on conventionally prepared smears. NSI's patents cover applications of
its technology to cytological screening for cancers occurring at all body sites,
and the Company's license of NSI's technology (described below) would extend to
these applications.
The foregoing information concerning NSI and the PAPNET(R) Testing
System was obtained either directlY from NSI or from filings that NSI has made
with the Commission. While the Company believes that the foregoing information
is accurate and a fair summary of publicly available information concerning NSI
and the PAPNET(R) Testing System, readers are encouraged to review NSI's filings
with the Commission for additional and more detailed information.
THE NSI LICENSE
On December 5, 1995 the Company, the Predecessor Companies, Cytology
West, Inc. and Papnet Utah, Inc. (other NSI regional licensees who were not
parties to the Merger), entered into the Settlement Agreement with NSI. The
purpose of the Settlement Agreement was to resolve and clarify certain issues
relating to the license agreements that NSI had with its regional licensees
(relating to, among other things, calculation of royalties, control of marketing
and sales activities, use of NSI's trademarks, and rights to market other
technologies developed by NSI), and issues relating to warrants to purchase
shares of NSI common stock which were held by the Company and certain of the
Predecessor Companies. Pursuant to the Settlement Agreement, NSI and the
regional licensees agreed to the form of a license agreement, under which the
Company and the other regional licensees will continue to have the rights to
market the PAPNET(R) Testing System, as well as certain other medicaL
technologies which may be developed by NSI ("NSI Technology").
While the Company and NSI have agreed on the form of a license
agreement, which the Company has agreed to execute with certain modifications,
no final agreement had been executed by the parties as of September 15, 1997.
The modifications requested by the Company deal principally with the
determination of the amount of royalties that should be paid to the Company with
respect to slides originating in its licensed territory but that are processed
by laboratories located outside of the territory. Although no final license
agreement has been executed, since the execution of the Settlement Agreement the
Company and NSI have in all material respects operated under the terms contained
in the form of license agreement incorporated in the Settlement Agreement.
The Company has the right and license to sell the PAPNET(R) Testing
System service and NSI Technology iN the states of Ohio, Georgia, Kentucky,
Missouri, North Carolina and in the Consolidated Metropolitan Statistical Area
of Chicago, Illinois. The Company's rights are exclusive within the described
territory, subject to the right of NSI to conduct marketing and sales activities
therein. However, because the royalties paid to the Company are based on
"Territory Gross Revenues" recognized by NSI from activities (including any
sales by NSI) in the licensed territory, any sales activities in the Company's
territory by NSI will inure to the benefit of the Company.
The form of license agreement incorporated in the Settlement Agreement
provides that the regional licensees (as a group) will be paid royalties as
follows: (a) monthly royalties equal to 50% of the amount by which NSI's gross
revenues from sales in the licensed territories exceed the cost of processing
slides originating in the licensed territories (for purposes of which
calculation costs per slide may not exceed $1.00 per slide) and the cost of
transporting such slides, with the maximum amount of such monthly royalties in
any fiscal year capped at an amount derived by applying the royalty formula to
12,175,000 slides; (b) annual royalties equal to the difference, if any, by
which aggregate monthly royalties in any fiscal year are less than 4.15% of
NSI's worldwide gross revenues for such fiscal year, with the maximum annual
royalty amount in any fiscal year capped at $23,000,000, less the amount of
monthly royalties paid in such fiscal year calculated as described in clause
(a). For the purposes of calculating the numbers of slides attributable to a
licensee's territory which are submitted by certain large laboratories operating
in
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multiple states ("Multistate National Laboratories"), there will be attributed
to each territory a proportionate number of slides submitted to NSI for
processing from all Multistate National Laboratories equal to the ratio that the
population of such territory bears to the population of the United States
(determined according to census data). These provisions may, in some
circumstances, have the effect of limiting the potential revenues which the
Company can realize from its sales activities.
The royalty calculations described in the foregoing paragraph are
aggregate calculations for all of the territorial licensees. Based upon the
aggregation of the applicable amounts contained in the original license
agreements of the Company and the Predecessor Companies and recent census data,
the Company believes that its share of the number of slides for the slide
royalty cap described in clause (a) in the foregoing paragraph will be
approximately 10,000,000 slides, the worldwide revenue percentage described in
clause (b) will be 3.5 percent, and the royalty cap described in the same clause
will be approximately $18.8 million.
The Company's license has an initial term that expires on December 31,
2025. The Company has the right to extend the license for an additional 20 year
term upon written notice to NSI within six months preceding the expiration of
the initial term and upon payment of a renewal fee, which is based on the net
present value at the time of such notice of 20 years of royalties at the average
monthly rate payable in the 12 months preceding the date of the notice. The
license may not be terminated or cancelled except upon expiration of its initial
or renewal term or by written agreement of the parties.
THIRD-PARTY REIMBURSEMENT
Reimbursement of laboratory charges for PAPNET(R) testing by
third-party medical insurance payers, manageD care organizations, and government
agencies (such as Medicare/Medicaid, private health insurance, health
maintenance organizations and self-insured employers) is a key factor in the
rate of growth of the revenues which NSI and the Company will be able to realize
from this technology. Currently, some third-party payers reimburse some or all
of the charges to patients for the PAPNET(R) test, others (including Medicare
and Medicaid) provide nO reimbursement. To the extent that third-party payers do
not provide for reimbursement of PAPNET(R) testing, or, iF the level of
reimbursement is significantly below the amount laboratories charge patients to
perform PAPNET(R) testing, the size of the potential market available to NSI and
the Company may be reduced. Based upon a study recently published in the
international journal Acta Cytologica finding that PAPNET(R) testing for
cervical canceR detection decreases the incidence of cervical cancer at a cost
which is within the range of tests and other procedures commonly reimbursed by
managed care organizations, the Company anticipates that it will eventually be
successful in convincing most third-party payers in its licensed territory to
reimburse for the PAPNET(R) test.
Consequently, the Company and NSI are directing their marketing efforts
to obtaining third-party reimbursement for the PAPNET(R) test. In February 1997,
the Company entered into an agreement with Medical MutuaL of Ohio, Inc. (MMO)
(formerly Blue Cross and Blue Shield of Ohio, Inc.) whereby MMO agreed to cover
the cost of the PAPNET(R) test for all members. In addition, MMO has agreed to
strongly recommend to its clinicians anD laboratories that all negative Pap
smears covered by its benefit plans are to be examined using PAPNET(R) testing.
MMO was the largest health care provider in the State of Ohio in 1996, with
approximately 1.5 million covered members. While the Company believes that its
agreement with MMO will increase the number of Pap smears from its licensed
territory which are processed using the PAPNET(R) System during 1997 and
subsequent years, there can be nO guarantee as to the amount or timing of any
increase.
OTHER COMPANY TECHNOLOGIES
The Company recently entered into an agreement with CeramPhysics, Inc.
of Westerville, Ohio ("Ceram"), pursuant to which the Company has the right to
acquire control of a newly-organized corporation holding a world-wide license to
Ceram's patented oxygen generation technology, which is exclusive as to all
applications of the technology except oxygen sensors and fuel cells. Pursuant to
the agreement, the Company will work with and loan up to $200,000 to Ceram to
complete the fabrication and testing of a ceramic element incorporating the
licensed technology, which will be capable of generating oxygen of a purity and
in quantities suitable for medical use. It is the Company's intention to
incorporate the element into an oxygen generation device that the Company will
manufacture and market for the home health care market. If the device is
acceptable to the Company, it has the right to acquire a 95% interest in the
licensee for an additional $200,000 investment, with the remaining 5% to be held
by
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Ceram. This new subsidiary would manufacture and market the device, as well as
pursue additional applications for the licensed technology.
The Company is currently negotiating for the rights in other medical
technologies, but has not concluded any binding agreements to date.
THE MERGER
On December 16, 1996, the Company completed the Merger with the
Predecessor Companies, which had collectively acquired the rights to market the
PAPNET(R) Testing System and service in the states of Missouri, Georgia, and
North Carolina. The Company was the surviving corporation in the Merger. Upon
completion of the Merger, the Company changed its name from Papnet of Ohio, Inc.
to NetMed, Inc.
Each of the Predecessor Companies, other than CCWP, Inc. was organized
to acquire and exercise the right to market the PAPNET(R) Testing System and
PAPNET(R) Service within its licensed territory. However, until November 8,
1995, when the United States Food and Drug Administration ("FDA") finally
approved the marketing of the Papnet(R) technology, the technology could be used
in the United States only for investigational purposes in connection with the
FDA approval process. Consequently, the Predecessor Companies had only limited
operations prior to November 1995. CCWP, Inc. was an affiliate of Carolina
Cytology, Inc. and was organized for the purpose of holding certain warrants for
the purchase of NSI common stock.
Cytology Indiana, Inc. ("CIN") was an Ohio corporation formed on
September 7, 1990. CIN owned an approximate 65% interest in the rights to market
the PAPNET(R) Testing System and service in Missouri. Indiana Cytology Review
Company ("INC") was an Ohio corporation formed on December 1, 1995, and owned an
approximate 35% interest in the PAPNET(R) marketing rights for Missouri. ER
Group, Inc. ("ERG") was an Ohio corporation formed oN May 13, 1991 for the
purpose of acquiring PAPNET(R) marketing rights for Georgia. Carolina Cytology,
Inc. ("CCI") was an Ohio corporation formed on December 10, 1992 for the purpose
of acquiring PAPNET(R) marketing rights foR North Carolina. CCWP Partners, Inc.
("CCWP") was an Ohio corporation formed on December 1, to hold certain warrants
to acquire NSI common stock acquired by a predecessor partnership in connection
with the acquisition of the PAPNET(R) marketing rights for North Carolina by
CCI.
In the Merger, all outstanding common shares of the Predecessor
Companies, including shares issuable upon the exercise of outstanding warrants
and options, were converted into the right to receive fully paid and
nonassessable common shares of the Company. Shares of outstanding common stock
of the Predecessor Companies were converted into Company shares based on a ratio
of one Predecessor Company share for the following number of shares of the
Company: CIN (1,121.6652); INC (4,491.7064); ERG (3,237.2643); CCWP (37.3971);
and CCI (1,487.6186). Immediately following the Merger, the shareholders of each
of the Predecessor Companies owned, in the aggregate, the following percentage
of the issued and outstanding stock of the Company: CIN (7.70%); INC (4.11%);
ERG (17.13%); CCWP (3.13%); and CCI (12.32%). Certain restrictions were imposed
on the resale of shares issued in the Merger, to be released over the one year
period following the Merger, which period may be accelerated by the Company. As
of the date of this Prospectus, such restrictions have expired as to 425,000
shares.
The merger of the Company and the Predecessor Companies was accounted
for at historical cost. For accounting purposes, Papnet of Ohio, Inc. is treated
as the predecessor of the merged entity and its historical financial statements
are included in this report as the historical financial statements of the
Company.
PERSONNEL
As of August 31, 1997, the Company employed sixteen (16) full time
employees. None of the Company's employees are subject to a collective
bargaining agreement, and the Company considers its relationship with its
employees to be good.
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FACILITIES
The Company's executive offices are located in Dublin, Ohio, in
approximately 4,900 square feet of space. The Company leases such space at an
annual net rent of $53,900. See "Certain Relationships and Related
Transactions."
MANAGEMENT
EXECUTIVE OFFICERS AND DIRECTORS
The executive officers and directors of the Company are as follows:
NAME AGE POSITION
---- --- --------
David J. Richards 46 Chairman, President and Chief Executive
Officer; Class I Director
John P. Kennedy 44 Vice President - Business Development;
Class II Director
Kenneth B. Leachman 44 Vice President - Finance; Chief Financial
Officer
William J. Kelly, Jr. 46 Vice President, General Counsel and
Secretary
Michael S. Blue, M.D. 41 Class I Director
S. Trevor Ferger 42 Class I Director
Robert J. Massey 51 Class II Director
Cecil J. Petitti 42 Class I Director
James F. Zid 63 Class II Director
The Company's Regulations provide for a classified board of directors
consisting of two classes, unless there are nine (9) or more directors, in which
case the Board will be divided into three classes. There are currently seven (7)
directors, therefore there are two classes of directors. Each class of directors
consists, as nearly as practical, of one-half of the total number of directors.
The term of office of the Class I directors will expire at the 1999 Annual
Meeting of Shareholders, and the term of the Class II directors will expire at
the 1998 Annual Meeting of Shareholders.
David J. Richards, a founder of the Company, has served as President
and director of the Company since its inception. From 1981 until commencing
employment with the Company, Mr. Richards was a practicing attorney and, from
1983, a partner, in the law firm of Crabbe, Brown, Jones, Potts & Schmidt in
Columbus, Ohio. From 1985 through 1994, Mr. Richards was engaged in real estate
development as President of Sunset Development, a multi-family housing
developer.
Mr. Richards has an accounting degree from Wright State University, and
earned his Juris Doctor degree from The Ohio State University College of Law in
1977.
John P. Kennedy is also a founder of the Company and has served as an
officer and director since its inception. Mr. Kennedy is currently Vice
President - Business Development. Until December 31, 1996, Mr. Kennedy was of
counsel with the law firm of Crabbe, Brown, Jones, Potts & Schmidt in Columbus,
Ohio, where he was a partner from 1986 to 1994. Mr. Kennedy has been a Columbus,
Ohio City Councilman since 1988, was President of Council from 1994 to 1996 and
is a director of Pugh Shows, Inc.
Mr. Kennedy has a Bachelor of Arts in Finance from the University of
Bridgeport, Bridgeport, Connecticut and earned his Juris Doctor from The Ohio
Northern University College of Law in 1978.
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Kenneth B. Leachman was elected as Vice President of Finance in October
1996. Mr. Leachman has held various financial management positions with several
technology based companies, including Corporate Controller for Goal Systems
International from 1989 to 1991 and as Chief Financial Officer of Sarcom, Inc.
from 1992 to 1994.
Mr. Leachman has a Bachelor of Science degree in accounting from The
Ohio State University in 1975 and earned his CPA certificate from the State of
Ohio in 1977.
William J. Kelly, Jr. was elected as Vice President, General Counsel
and Secretary in July 1997. Prior to joining the Company, he practiced law with
the firm of Porter, Wright, Morris & Arthur in Columbus, Ohio, where he was a
partner since 1983. Mr. Kelly earned a Bachelor of Arts degree from The Ohio
State University in 1973, and a Juris Doctor degree from The Ohio State
University College of Law in 1976.
Michael S. Blue, M.D. has been a practicing physician since 1980. Dr.
Blue graduated from Miami University of Ohio in 1976 with a Bachelor of Science
in Zoology and graduated from The Ohio State University with a Doctor of
Medicine in 1979. Dr. Blue has been President of Phoenix Group International,
Ltd. and North American International Trade Group, Inc. since 1994 and 1992,
respectively. He has also been Secretary/Treasurer and member of the Board of
Directors of Columbus Oilfield Exploration, Inc. since 1987. Dr. Blue has been a
director of the Company since December 1996.
Robert J. Massey has served on the Board of Directors of the Company
since January, 1997. He is the past President and Chief Executive Officer of
CompuServe Corporation, an office he retained for one and a half years. Prior to
serving as CompuServe's CEO, Mr. Massey held numerous executive positions with
the firm over a twenty year period in various sales, marketing and general
management areas of responsibility, plus served on the company's Board of
Directors during the period 1991 through 1997. Mr. Massey also was a sales
manager with RIM and Control Data Corporation. He is a graduate of Holy Cross
College, Worchester, Massachusetts and received an MBA in Finance from Syracuse
University. He is currently President of RJM & Associates, a Columbus, Ohio
based consulting firm.
S. Trevor Ferger is President of Ferger & Associates, a master broker
specializing in the sales and marketing of consumer goods to grocery stores. He
also serves as Director of Sales for Acosta Sales Company, a marketer of
consumer products. Mr. Ferger has been active with Ferger & Associates since
1979. Prior to that time he was a sales manager with Procter & Gamble. Mr.
Ferger has a Bachelor of Arts degree from Wake Forest University and a M.B.A.
degree from Xavier University. Mr. Ferger has been a director of the Company
since June, 1994.
Cecil J. Petitti has been co-owner of Chaney & Petitti Insurance Agency
located in Dublin, Ohio since 1984. Chaney & Petitti specialize in multiple
insurance products, including medical insurance. Prior to merging with the
Chaney Group, Mr. Petitti was associated with the Burke, Kendall & Petitti
Insurance Agency. Mr. Petitti is also President of NetWalk, Inc., a
Columbus-based Internet service provider. Mr. Petitti earned a Bachelor of Arts
degree in Education from The Ohio State University. Mr. Petitti has been a
director of the Company since June, 1994.
James F. Zid has served on the Board of Directors of the Company since
February, 1997. Mr. Zid retired as the managing partner of the Columbus office
of Ernst & Young LLP in 1993. While at Ernst & Young Mr. Zid worked with clients
in the banking, health care, insurance, and manufacturing industries. Mr. Zid
has served on the Board of Directors of the Greater Columbus Chamber of
Commerce, the Health Coalition of Central Ohio, the Franklin County Academy of
Medicine Foundation, and the Columbus Museum of Art. Mr. Zid currently serves on
the Board of Directors of Neoprobe Corporation and Central Benefits Insurance
Company.
COMMITTEES OF THE BOARD
Prior to December 1996, the Board of Directors had no standing
committees, and all corporate decisions were made by the entire Board. Following
the Merger, the Board appointed an Audit Committee consisting of Messrs.
Richards, Blue and Ferger and a Compensation Committee consisting Messrs. Blue,
Petitti, and Massey. The Audit Committee is charged with reviewing the Company's
annual audit and meeting with the Company's independent accountants to review
the Company's internal controls and financial management practices.
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The Compensation Committee has the authority and responsibility to determine and
administer the Company's officer compensation policies and to establish the
salaries for executive officers, the formula for bonus awards to executive
officers, and the grant of stock options to executive officers and other key
employees under the Company's 1995 Amended and Restated Stock Option Plan (the
"Option Plan").
EXECUTIVE COMPENSATION
The following table sets forth certain information regarding
compensation paid during fiscal 1996 to the Company's President, who was the
only executive officer whose annual salary and bonus exceeded $100,000 for each
of the Company's last three fiscal years ended December 31, 1996 (the "Named
Executive Officer").
SUMMARY COMPENSATION TABLE
LONG-TERM
ANNUAL COMPENSATION COMPENSATION
-------------------------- ------------
AWARDS
------------ ALL OTHER
NAME AND PRINCIPAL POSITION YEAR SALARY BONUS SECURITIES COMPENSATION
($) ($) UNDERLYING ($)(1)
OPTIONS
(#)
- --------------------------------- ---- -------- ---------- ---------- -------
David J. Richards, President 1996 $125,000 $100,000(2) 0 $9,338
1995 $125,000 0 0 $12,228
1994 $108,333 0 0 $8,900
<FN>
(1) Includes matching contribution to the Company's 401(k) Plan and car
allowance.
(2) Consists of a $50,000 cash bonus for 1995, which was paid in 1996 and
$50,000 represented by the forgiveness of indebtedness to the Company,
which was approved by the Board of Directors in 1995 and conditioned on
completion of the Merger.
OPTION/SAR GRANTS IN LAST FISCAL YEAR
There were no options granted to the Named Executive Officer during the
fiscal year ended 1996.
AGGREGATED OPTION EXERCISES AND FISCAL YEAR-END OPTION VALUE TABLE
The following table provides certain information regarding the number and
value of stock options held by the Named Executive Officer at December 31, 1996.
AGGREGATED OPTION EXERCISES IN LAST FISCAL YEAR
AND FISCAL YEAR-END OPTION VALUES
NUMBER OF SECURITIES VALUE OF UNEXERCISED
UNDERLYING UNEXERCISED IN-THE-MONEY OPTIONS AT
OPTIONS AT FISCAL YEAR-END (#) FISCAL YEAR-END ($)(1)
---------------------------- ----------------------------
SHARES VALUE EXERCISABLE UNEXERCISABLE EXERCISABLE UNEXERCISABLE
NAME ACQUIRED REALIZED
ON ($)
EXERCISE
(#)
- ------------------ --------- --------- ----------- ------------- ------------ -------------
David J. Richards -- -- 287,020 -- $2,028,395 --
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(1) Represents the total gain which would be realized if all in-the-money
options held at year end were exercised, determined by multiplying the
number of shares underlying the options by the difference between the per
share option exercise price and the per share fair market value at year end
($8.125 on December 31, 1996). An option is in-the-money if the fair market
value of the underlying shares exceeds the exercise price of the option.
COMPENSATION OF DIRECTORS
Directors who are not employees of the Company receive no cash
compensation or expense reimbursement for their services, but receive stock
options as compensation for their services. The exercise price for options
granted in 1996 and prior years ranges from $3.25 to $11.00 per share. In
February 1997, each non-employee director received options to purchase 2,000
common shares, exercisable at $8.40 per share for their services in 1996. Such
options are currently exercisable and will terminate 10 years from the date of
grant. Subsequently, Messrs. Ferger, Petitti and Blue were each granted options
for 20,000 shares (exercisable at $7.54 per share), and Messrs. Massey and Zid
were each granted options for 25,000 shares (exercisable at $6.16 per share in
the case of Mr. Massey and at $6.20 per share in the case of Mr. Zid). The
latter options were granted in consideration for service during 1997, 1998, and
1999, will vest at the rate of one-third of the shares at the end of each year,
and will terminate 10 years from the date of grant.
EMPLOYMENT AGREEMENTS
Effective April 1, 1997, the Company entered into an employment
agreement with Mr. Richards, its President and Chief Executive Officer. The
Agreement is for a term of three years, and provides for annual base salary of
$225,000 during the term. In addition to the base salary, the agreement provides
that Mr. Richards will receive an annual incentive bonus of up to 100% of his
base salary, to be determined according to performance criteria established by
the Board or its Compensation Committee, as well as an automobile allowance,
Company-provided term insurance in a minimum face amount of $1,000,000, and
other benefits.
The agreement also provides for the grant, pursuant to the Option Plan,
of options to purchase 150,000 common shares, vesting at the rate of 50,000
shares per employment year during the term, with exercise prices ranging from
$6.94 per share to $12.00 per share. The agreement provides that, in the event
that Mr. Richards' employment is terminated other than for good cause (as
defined in the agreement), or is constructively terminated, the Company will
continue his base salary and health insurance coverage for a period of 18 months
after termination and pay any earned but unpaid incentive bonus, and that the
options granted pursuant to the agreement will become immediately exercisable.
For purposes of the agreement, a constructive termination is defined as removal
of Mr. Richards as President, Chief Executive Officer or a Director of the
Company, or a substantial change in his duties or reporting responsibility to
the Board. In the event of a "Change of Control" (as defined in the Agreement),
Mr. Richards may voluntarily terminate his employment at any time within one
year thereafter, if (i) he determines in good faith that as a result of the
Change of Control he can no longer adequately exercise the authority, powers,
functions or duties of a chief executive officer, or can no longer perform such
duties by reason of a substantial diminution in his responsibilities, status,
perquisites or position, or (ii) the Company materially breaches or fails to
assume any material obligation under the agreement. In the event of such
termination, the Company will pay Mr. Richards 18 months of base salary in a
lump sum, reimbursement of any previously unreimbursed business expenses, and an
amount equal to the greater of (A) the full incentive bonus for which he could
receive under any bonus criteria established by the Board of Directors for the
employment year in which termination occurs (regardless of whether such criteria
are actually satisfied), or (B) the incentive bonus actually paid to him during
the previous employment year. In addition, the Company must continue his health
insurance benefits for a period of 18 months, and the options granted pursuant
to the agreement will become immediately exercisable. The foregoing obligations
of the Company also apply in the event that Mr. Richards' employment is
terminated by the Company other than for cause within one (1) year following a
Change of Control.
In the event of Mr. Richards' death during the employment term, in
addition to the payment of salary and bonus earned to the date of death, and the
immediate exercisability of stock options, the agreement provides that the
Company will purchase from his estate of up to $2 million in market value of
common shares of the Company owned by Mr. Richards on the date of death. The
agreement requires the Company to purchase and pay the premiums on a policy of
key man life insurance sufficient to fund such obligation. Finally, the
agreement imposes
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confidentiality and noncompetition obligations on Mr. Richards, and requires
that he assign to the Company any intellectual property (inventions, trade
secrets, works of authorship, and the like) created by him during his employment
which is useful in the Company's business.
Effective July 1997, the Company entered into an employment agreement
with Mr. Kelly, employing him as Vice President, General Counsel and Secretary
for a term of three years. The material terms of the agreement with Mr. Kelly
are comparable to those contained in the agreement with Mr. Richards, except
that the annual base salary is $170,000, the grant of stock options is for
75,000 shares at prices ranging from $8.00 to $12.00 per share, no term life
insurance (except pursuant to Company plans applicable to all executives) or
automobile allowance is provided, no provisions are included which would impose
obligations on the Company in the event of a constructive termination of Mr.
Kelly's employment, and the Company has no obligation to repurchase any common
shares of the Company owned by Mr. Kelly upon his death.
STOCK OPTION PLAN
The Option Plan was adopted by the Board of Directors and approved by
the shareholders in September 1995. The Option Plan was later amended to make
changes to facilitate compliance with Section 16 of the Securities Act of 1934,
and was most recently amended in May 1997 by the shareholders to increase the
number of shares for which options could be granted under the Option Plan.
Options granted under the Option Plan may either meet the requirements of
Section 422 ("Incentive Options") of the Internal Revenue Code of 1986, as
amended (the "Code") or not meet such requirements ("Nonqualified Options"). Key
employees, officers, and directors of, and consultants and advisors who render
services to, the Company are eligible to receive options under the Option Plan.
The Option Plan may be administered by the Board of Directors or a
Stock Option and Compensation Committee (the "Committee") consisting of
directors who are not employees of the Company. The Board or Committee
determines the number of shares subject to option, the duration of the option,
the per share exercise price, the rate and manner of exercise, and whether the
option is intended to be a Nonqualified Option or an Incentive Option. An
incentive Option may not have an exercise price less than fair market value of
the Company's common stock on the date of grant or an exercise period that
exceeds ten years from the date of grant and is subject to certain other
limitations which allow the option holder to qualify for favorable tax
treatment. None of these restrictions applies to the grant of Nonqualified
Options, which may have an exercise price less than the fair market value of the
underlying common stock on the date of grant and may be exercisable for an
indeterminate period of time. The Board or Committee also has the discretion
under the Option Plan to make cash grants to option holders that are intended to
offset a portion of the taxes payable upon exercise of Nonqualified Options or
on certain dispositions of shares acquired under Incentive Options.
To date, the criteria applied by the Board of Directors and its
Compensation Committee in determining the eligibility, amount, exercise price,
and the vesting of stock options awarded under the Option Plan have been
determined on a case-by-case basis. While no specific formula has been adopted,
the Board and Committee have considered performance, overall contribution to the
Company, the number of vested and unvested stock options already held and other
similar factors in awarding stock options.
The exercise price of the option may be paid in cash or, with the
consent of the Board or Committee, (i) with previously acquired shares of common
stock valued at their fair market value on the date they are tendered, (ii)
delivery of a full recourse promissory note, the terms and conditions of which
will be determined by the Board, or (iii) by delivery of written instructions to
forward the notice of exercise to a broker or dealer and to deliver to a
specified account a certificate for the shares purchased upon exercise of the
option and a copy of irrevocable instructions to the broker or dealer to deliver
the purchase price of the shares to the Company.
Any option granted under the Option Plan will terminate automatically
(i) 30 days after an employee's termination of employment with the Company
(other than by reason of death or disability or for cause), and (ii) one year
after the employee's death or termination of employment by reason of disability,
unless the option expires earlier by its terms. Options not exercisable as of
the date of a change in control of the Company will become exercisable
immediately as of such date. Options granted under the Plan are not transferable
except by will or the laws of descent and distribution.
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The Board may amend or modify the Plan at any time provided that (a) no
amendment may be made to the Plan which would cause the Incentive Options
granted thereunder to fail to qualify as incentive stock options under the Code;
and (b) any amendment which requires the approval of the shareholders of the
Company under the Code or Section 16 of the Securities Exchange Act of 1934, as
amended, or the regulations promulgated thereunder, will be subject to such
approval in accordance with the applicable law or regulations. No amendment,
modification or termination of the Plan may in any manner adversely affect any
option previously granted under the Plan without the consent of the option
holder or a permitted transferee of such option holder.
As of August 31, 1997, the following current directors and executive
officers had been granted options under the Plan:
NAME NUMBER OF OPTIONS GRANTED AVERAGE EXERCISE PRICE PER SHARE
---- ------------------------- --------------------------------
David J. Richards 150,000 $ 9.65
Kenneth B. Leachman 50,000 $ 5.95
William J. Kelly, Jr 75,000 $ 10.00
Robert J. Massey 25,000 $ 6.16
John P. Kennedy 102,000 $ 7.04
S. Trevor Ferger 22,000 $ 7.62
Cecil J. Petitti 22,000 $ 7.62
James F. Zid 25,000 $ 6.20
Michael S. Blue 20,000 $ 7.54
OWNERSHIP OF COMMON STOCK BY MANAGEMENT AND PRINCIPAL SHAREHOLDERS
The following table sets forth information regarding beneficial
ownership of the Common Stock by each director and executive officer, each
person known by the Company to own beneficially more than 5% of the outstanding
Common Stock, and the directors and executive officers of the Company as a group
as of August 31, 1997:
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SHARES BENEFICIALLY OWNED (1)
-----------------------------
NAME OF BENEFICIAL OWNER NUMBER PERCENT
- ----------------------------------------- ------------- -----------
David J. Richards(2) 1,520,000 13.5
John P. Kennedy(3) 662,244 6.0
Kenneth B. Leachman 1,000 *
William J. Kelly, Jr 2,000 *
S. Trevor Ferger(4) 293,825 2.7
Cecil J. Petitti(5) 165,976 1.5
Michael S. Blue 286,717 2.6
Robert J. Massey 48,922 *
James F. Zid 3,800 *
Rodney M. Kinsey(6) 617,085 5.5
Carl Genberg(7) 695,000 6.2
All directors and executive officers as a group
(9 persons) 2,987,036 26.5
<FN>
- ----------
* Represents beneficial ownership of less than 1% of the Company's
outstanding Common Stock.
(1) Beneficial ownership is determined in accordance with the rules of the
Commission which generally attribute beneficial ownership of securities to
persons who possess sole or shared voting power and/or investment power or
as to which the person has the right to acquire the beneficial ownership
within 60 days of August 31, 1997. Unless otherwise indicated, voting power
and investment power are exercised solely by the person named above or
shared with members of his household.
(2) Includes 287,020 shares that may be purchased under stock options
exercisable within 60 days of August 31, 1997.
(3) Includes 26,000 shares that may be purchased under stock option exercisable
within 60 days of August 31, 1997.
(4) Includes 10,000 shares that may be purchased under stock options
exercisable within 60 days of August 31, 1997, and 99,849 shares held in
trust for the benefit of Mr. Ferger's children.
(5) Includes 10,000 shares that may be purchased under stock options
exercisable within 60 days of August 31, 1997.
(6) Includes 494,385 held of record by Mr. Kinsey, 80,331 shares held by Mr.
Kinsey's wife, and 35,702 shares held by his children. Mr. Kinsey resigned
from the board of directors effective February 26, 1997. Mr.
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Kinsey's address is 8651 Gairloch Ct., Dublin, Ohio 43017. Also
includes 6,667 shares that may be purchased under stock options exercisable
within 60 days of August 31, 1997.
(7) Mr. Genberg's address is 101 Convention Center Drive, Suite 1001, Las
Vegas, Nevada 89109.
CERTAIN RELATIONSHIPS AND RELATED TRANSACTIONS
In December 1996 the Company completed the Merger with the Predecessor
Companies, which had acquired the rights to market the PAPNET(R) System in the
states of Missouri, Georgia, and North Carolina. The Company was the surviving
corporation in the Merger. Upon completion of the Merger, the Company changed
its name from Papnet of Ohio, Inc. to NetMed, Inc.
The Company entered into a loan agreement, dated March 14, 1996 with
Cytology West, Inc. ("CWI") and Papnet Utah, Inc. ("PUI"). CWI is licensed to
sell the PAPNET(R) Testing System and the PAPNET(R) service in Arizona, Nevada
and San Diego County California. PUI is licensed to sell PAPNET(R) Testing
System and the PAPNET(R) Service in Utah. Carl Genberg, President of CWI, owns
695,000 shares of the Company's common stock. CWI and PUI were originally to
have been parties to a merger with the Company and the Predecessor Companies,
but that transaction was abandoned by the parties. CWI and PUI abandoned the
transaction in order to pursue other technologies that the Company and the
Predecessor Companies were not ready to pursue without assurances of the ability
to obtain the financing necessary to commercialize them. The loan agreement
provided for advances to CWI of up to $585,000 to cover certain operating
expenses, expenses associated with the abandoned merger, and the acquisition of
new technology. No specific amount was established for advances to PUI. The
advances bear interest at the rate of 7% per annum. No further advances will be
made under the loan agreement and as of December 31, 1996, the balance due was
$130,143. CWI has agreed to transfer 16,331 shares of NetMed common stock to the
Company in exchange for the cancellation of the outstanding balance.
In September 1997, the Company entered into a net lease with Muirfield
Square, Ltd. for 4,900 square feet of office space in which the Company's
principal offices are located. The lease term is for 5 years at an annual rent
of $53,900 for the first year, escalating annually at the rate of 3% over the
term, and renewable for an additional 5-year term at an annual net rental of
$60,660. Messrs. Richards, Ferger, and Massey own a majority of the membership
interests in Muirfield Square, Ltd. The Company believes that the lease is on
terms at least as favorable to the Company as available for office space of a
similar size and quality in the locality.
SELLING SHAREHOLDERS
The 1,500,000 shares of the Company's Common Stock described in this
Prospectus equal approximately 150% of the number of shares which would be
issuable upon conversion of the Debentures if the entire principal amount of the
Debentures was converted on the date of this Prospectus, plus the number of
Shares which would be issuable if the all of the Warrants were exercised on the
date of this Prospectus. Except for the ownership of the Debentures and Warrants
(and any Shares on conversion or exercise thereof), the Selling Shareholders
have not had any material relationship within the past three years with the
Company. The Shares are being registered to permit public secondary trading of
the Shares, and the Selling Shareholders may offer the Shares for resale from
time to time. See "Plan of Distribution."
The Shares being offered by the Selling Shareholders hereby are
issuable by the Company to the Selling Shareholders upon conversion of the
Debentures and exercise of the Warrants. The Debentures and Warrants were issued
by the Company on August 13, 1997 to the Selling Shareholders pursuant the
Purchase Agreements. The Debentures and any interest accrued thereon may be
converted into Shares at any time. However, no sales of Shares may be made prior
to November 11, 1997, and during the period from November 11, 1997 through May
10, 1998 (the 91st through 270th day after the closing) the maximum aggregate
number of Shares which can be sold is 500,000. After May 10, 1998 (the 270th day
after the closing), 100% of the Shares may be sold. The Company can prohibit
sales during the "Blackout Period. The Debentures bear interest at 6% per annum,
payable in Common Stock of the Company at the time of each conversion, and are
convertible into shares of the Company's Common Stock based on the "Conversion
Price" at the time of conversion. The "Conversion Price" varies based on the
date when the Debentures are converted. For the period through March 31, 1998,
the Conversion Price is an amount
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equal to 80% of the average closing bid price of the Common Stock on the
American Stock Exchange for the previous three business days ending on the day
before the conversion date. For the period beginning April 1, 1998, the
Conversion Price is an amount equal to 75% of the average closing bid price of
the Common Stock on the American Stock Exchange for the previous three business
days ending on the day before the conversion date. The Conversion Price is
subject to equitable adjustment upon the occurrence of certain events, such as
stock splits, stock dividends, reclassifications or combinations.
If not previously converted, the entire outstanding principal and
interest on the Debentures will be automatically converted to Common Stock on
August 13, 2000 (the third anniversary of the closing). Notwithstanding the
foregoing, a Selling Shareholder is prohibited from converting any portion of
the Debentures which would result in the Selling Shareholder being deemed the
beneficial owner, in accordance with the provisions of Rule 13d-3 of the
Securities Exchange Act of 1934, as amended, of 4.99% or more of the then issued
and outstanding Common Stock of the Company.
The Warrants are exercisable at any time prior to August 13, 2000 at
exercise prices of $7.79 per Share (for up to 150,000 Shares) and $9.35 per
Share (for up to 65,000 Shares).
The Debentures are secured by 475,000 shares of common stock of
Neuromedical Systems, Inc. (Nasdaq: NSIX) owned by the Company (the "NSI
Shares"). If at any time prior to March 31, 1998, the conversion price is $3.00
or less, the holders of the Debentures may elect to exercise their conversion
rights for NSI Shares, rather than Common Stock of the Company, at a 20%
discount from the market price at the time of conversion.. If the Company
prohibits conversions during the Blackout Period, and the trading volume in the
Common Stock prior to December 15, 1997 does not meet defined minimums, the
holders may convert into the NSI Shares at a discount from the market price
which would produce a 25% return on an annualized basis. The NSI Shares may be
released from the pledge ratably as the outstanding principal amount of
Debentures is reduced.
As required by the Purchase Agreements and related Registration Rights
Agreements, in recognition of the fact that Selling Shareholders may wish to be
legally permitted to sell any Shares acquired upon conversion of the Debentures
and exercise of the Warrants when they deem appropriate, the Company has filed
with the Commission under the Act a Registration Statement on Form S-1, of which
this Prospectus forms a part, with respect to the resale of the Shares by the
Selling Shareholders from time to time on the American Stock Exchange or in
privately-negotiated transactions.
NAME OF SELLING SHAREHOLDER NUMBER OF SHARES BENEFICIALLY NUMBER OF SHARES BEING NUMBER OF SHARES BENEFICIALLY
OWNED PRIOR TO OFFERING* OFFERED HEREBY OWNED AFTER OFFERING
CPR (USA), Inc. 1,015,667 1,015,667 0
LibertyView Fund, LLC 277,333 277,333 0
LibertyView Plus Fund 91,999 91,999 0
Goodbody International, Inc. 100,000 100,000 0
Clarco Holdings, Inc. 15,000 15,000 0
<FN>
*Represents approximately 150% of the aggregate number of shares of the
Company's Common Stock which the Selling Shareholders would be entitled to
acquire upon conversion of the Debentures assuming the entire principal and
interest on the Debentures was converted on the date of this Prospectus, plus
the number of shares issuable assuming the Warrants are fully exercised. The
Selling Shareholders do not currently own any shares and the actual number of
shares which will be beneficially owned by the Selling Shareholders after
conversion of the Debentures will depend on the conversion price on the date the
debentures are converted.
PLAN OF DISTRIBUTION
The Shares being offered by the Selling Shareholders will be sold in
one or more transactions (which may involve block transactions) on the American
Stock Exchange or in privately-negotiated transactions. The sale price to the
public may be the market price prevailing at the time of sale, a price related
to such prevailing market price or such other price as each Selling Shareholder
determines from time to time. A Selling Shareholder shall have the sole and
absolute discretion not to accept any purchase offer or make any sale of Shares
if it deems the purchase price to be unsatisfactory at any particular time.
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The Selling Shareholders may also sell the Shares of Common Stock
directly to market makers acting as principals and/or to broker-dealers acting
as agents for themselves or their customers. Brokers acting as agents for the
Selling Shareholders will receive usual and customary commissions for brokerage
transactions, and market makers and block purchasers purchasing the Shares will
do so for their own account and at their own risk. It is possible that the
Selling Shareholders will attempt to sell Shares of Common Stock in block
transactions to market makers or other purchasers at a price per share which may
be below the then market price. There can be no assurance that all or any of the
Shares offered hereby will be issued to, or sold by, the Selling Shareholders.
The Selling Shareholders and any brokers, dealers or agents, upon effecting the
sale of any of the Shares offered hereby, may be deemed "underwriters" as that
term is defined in the Securities Act.
The Selling Shareholders have agreed that they will not pay more than
the normal brokerage compensation and that they will not enter into arrangements
for special selling efforts without first advising the Company and cooperating
in the disclosure of the same in a revised or supplemental prospectus.
The Selling Shareholders, alternatively, may sell all or any part of
the Shares offered hereby through an underwriter. The Selling Shareholders have
not entered into any agreement with a prospective underwriter and there is no
assurance that any such agreement will be entered into. If the Selling
Shareholders enters into such an agreement or agreements, the relevant details
will be set forth in a supplement or revisions to this Prospectus.
DESCRIPTION OF CAPITAL STOCK
The authorized capital stock of the Company consists of 20,000,000
Common Shares, without par value, 250,000 shares of Voting Preferred Stock, and
250,000 Shares of Nonvoting Preferred Stock. There are currently outstanding
10,947,114 shares of Common Stock, and no shares of preferred stock. All
outstanding shares of Common Stock are fully paid and non-assessable.
COMMON STOCK
Holders of validly issued and outstanding shares of Common Stock are
entitled to one vote per share of record on all matters to be voted upon by
shareholders. At a meeting of shareholders at which a quorum is present, a
majority of the votes cast decides all questions, unless the matter is one upon
which a different vote is required by express provision of law or the Company's
Articles of Incorporation ("Articles") or Code of Regulations ("Regulations").
The Company's Articles eliminate the right of shareholders to cumulate their
votes in the election of directors. Shareholders have no preemptive or other
rights to subscribe for additional shares nor any other rights to convert their
Company common stock into any other securities.
Subject to the preferences that may be applicable to the holders of any
outstanding shares of Preferred Stock, holders of common stock are entitled to
such dividends as may be declared by the Board of Directors out of funds legally
available therefor. The payment by the Company of dividends, if any, rests
within the discretion of its Board of Directors and will depend upon the
Company's operating results, financial condition and capital expenditure plans,
as well as other factors considered relevant by the Board of Directors. The
Company may enter into bank credit agreements which include financial covenants
restricting the payment of dividends. See "Dividend Policy."
Upon liquidation, dissolution or winding-up of the Company, the assets
legally available for distribution to shareholders are distributable ratably
among the holders of Company common stock at that time outstanding, subject to
prior distribution rights of creditors of the Company and preferential rights of
any outstanding shares of Preferred Stock.
PREFERRED STOCK
The Articles authorize the Board of Directors to issue up to 250,000
shares of Voting Preferred Stock and up to 250,000 shares of Nonvoting Preferred
Stock in one or more series and to establish such relative dividend, redemption,
liquidation, conversion and other powers, preferences, rights, qualifications,
limitations and restrictions as the Board of Directors may determine without
further approval of the shareholders of the Company. The issuance of Preferred
Stock by the Board of Directors could be used, under certain circumstances, as a
method of delaying or
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preventing a change in control of the Company and could permit the Board of
Directors, without any action by holders of Common Stock, to issue Preferred
Stock which could have a detrimental effect on the rights of holders of Common
Stock, including loss of voting control. In certain circumstances, this could
have the effect of decreasing the market price of the Common Stock.
The issuance of any series of Preferred Stock, and the relative powers,
preferences, rights, qualifications, limitations and restrictions of such
series, if and when established, will depend upon, among other things, the
future capital needs of the Company, the then-existing market conditions and
other factors that, in the judgment of the Company Board of Directors, might
warrant the issuance of Preferred Stock. At the date of this Prospectus, there
are no plans, agreements or understandings relative to the issuance of any
shares of Preferred Stock.
CERTAIN PROVISIONS OF ARTICLES AND REGULATIONS
The following brief description of certain provisions of the Company's
Articles and Regulations does not purport to be complete and is subject in all
respects to the provisions of the Articles and Regulations, copies of which have
been filed as exhibits to the Registration Statement of which this Prospectus is
a part.
CLASSIFIED BOARD OF DIRECTORS
The Company's Regulations provide for the Board of Directors to be
divided into three classes (unless there are fewer than 9 directors in which
case there will be two classes) of directors serving staggered three-year terms.
As a result, approximately one-third of the Board of Directors will be elected
each year. Classification of the Board of Directors expands the time required to
change the composition of a majority of directors and may tend to discourage a
proxy contest or other takeover bid for the Company.
DIRECTORS' RESPONSE TO ACQUISITION PROPOSALS
The Company's Articles provide that the Company Board of Directors must
base the response of the Company to any "Acquisition Proposal" on the Company
Board of Directors' evaluation of what is in the best interest of the Company.
In evaluating what is in the best interest of the Company, the Board of
Directors must consider all relevant factors including, without limitation, the
best interest of the shareholders which, for this purpose, requires the Board of
Directors to consider, among other factors, not only the consideration offered
in the Acquisition Proposal in relation to the then current market price of the
Company's stock, but also in relation to the current value of the Company in a
freely negotiated transaction and in relation to the Board of Directors' then
estimate of the future value of the Company as an independent entity or as the
subject of a future Acquisition Proposal; and such other factors as the Board of
Directors determines to be relevant, including, among other factors, the
long-term and short-term interests of the Company and its subsidiaries and their
businesses and properties and the social, legal and economic effects upon the
employees, suppliers, customers, creditors and other affected persons, firms and
corporations and on the communities and geographical areas in which the Company
and its subsidiaries operate or are located. "Acquisition Proposal" is defined
in the Articles as any proposal for the consolidation or merger of the Company
with another corporation, any share exchange involving the Company's outstanding
capital stock, any liquidation or dissolution of the Company, any transfer of
all or a material portion of the assets of the Company and any tender offer or
exchange offer for any of the Company's outstanding stock.
DIRECTOR AND OFFICER INDEMNIFICATION
The Articles provide that the Company may indemnify any director,
officer, or any former director or officer, and any person who is or has served
at the request of the Company as a director, officer or trustee of another
corporation, partnership, joint venture, trust or other enterprise (and his or
hers heirs, executors and administrators) against expenses, including attorney
fees, judgments, fines and amounts paid in settlement, actually and reasonably
incurred by him by reason of the fact that he is or was such director, officer,
incorporator or trustee in connection with any threatened, pending or completed
action, suit or proceeding, whether civil, criminal, administrative, or
investigative, to the full extent and according to the procedures and
requirements set forth in the Ohio General Corporation Law as the same may be in
effect from time to time. The indemnification provided shall not be deemed to
restrict the right of the Company to (i) indemnify employees, agents and others
as permitted by law, (ii) purchase and maintain insurance or provide similar
protection on behalf of the directors, officers or such other persons against
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liabilities asserted against them or expenses incurred by them arising out of
their service to the Company, and (iii) enter into agreements with such
directors, officers, employees, agents or others indemnifying them against any
and all liabilities asserted against them or incurred by them arising out of
their service to the Company as contemplated herein.
REMOVAL OF DIRECTORS
The Company's Regulations provide that any director or the entire Board
of Directors may be removed from office at any time, but only for cause and only
by the affirmative vote of the holders of at least 80% of all of the outstanding
shares of capital stock of the Company entitled to vote on the election of
directors at a meeting of shareholders called for that purpose, except that if
the Board of Directors, by an affirmative vote of at least 66 2/3% of the entire
Board, recommends removal of a director to the shareholders, such removal may be
effected by the affirmative vote of the holders of at least a majority of the
outstanding shares of capital stock of the Company present in person or
represented by proxy and entitled to vote on the election of directors at a
meeting of shareholders called for that purpose. These provisions, when coupled
with provisions of the Regulations authorizing only the Board of Directors to
fill vacant directorships, will preclude shareholders of the Company from
removing incumbent directors without cause, and simultaneously gaining control
of the Board of Directors by filling the vacancies with their own nominees.
The term "cause" is not defined in the Articles or the Ohio General
Corporation Law. Consequently, any question concerning the legal standard for
"cause" would have to be judicially determined and such a determination could be
difficult, expensive and time consuming.
MEETINGS OF SHAREHOLDERS
The Regulations provide that annual meetings of shareholders shall be
held at such time and on such business day as the Board of Directors may
determine. Except as otherwise provided by law or by the Articles, a quorum for
any meeting of the shareholders is a majority of the capital stock issued and
outstanding and entitled to vote at the meeting. Special meetings of
shareholders may be called by the Chairman of the Board, President or Chief
Executive Officer or by the Board of Directors by action at a meeting or a
majority of the directors without a meeting or by shareholders holding 50% or
more of the voting power entitled to elect directors.
ADVANCE NOTICE REQUIREMENTS FOR SHAREHOLDER PROPOSALS AND DIRECTOR NOMINATIONS
The Regulations provide that shareholders seeking to bring business
before a meeting of shareholders, or to nominate candidates for election as
directors at a meeting of shareholders, must provide timely notice thereof in
writing. To be timely, a shareholder's notice must be delivered to, or mailed
and received at, the principal executive office of the Company, not less than 30
days nor more than 60 days prior to the scheduled meeting (or, if less than 40
days' notice of the meeting is given to shareholders not later than the close of
business on the tenth day following the earlier of (i) the day on which such
notice of the date of the meeting was mailed, or (ii) the day on which public
disclosure of the date of the special meeting was made). The Regulations also
specify certain requirements pertaining to the form and substance of a
shareholder's notice. These provisions may preclude some shareholders from
making nominations for directors at an annual or special meeting or from
bringing other matters before the shareholders at a meeting.
VOTING REQUIREMENTS
The Regulations provide that certain provisions in the Regulations may
not be altered, amended or repealed in any respect, and new provisions
inconsistent therewith may not be adopted unless such action is approved by the
affirmative vote of the holders of at least 80% of all of the outstanding shares
of capital stock of the Company entitled to vote on such matter at a meeting of
shareholders called for that purpose.
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SHAREHOLDER NOMINATIONS AND PROPOSALS
The Regulations also specify certain requirements pertaining to the
form and substance of a shareholder's notice. These provisions may preclude some
shareholders from making nominations for directors at an annual or special
meeting or from bringing other matters before the shareholders at a meeting.
Although the Articles and Regulations do not give the Board of
Directors any power to approve or disapprove shareholder nominations for the
election of directors or proposals for action, the foregoing provisions may have
the effect of precluding a contest for the election of directors or the
consideration of shareholder proposals if the proper procedures are not
followed, and of discouraging or deterring a third party from conducting a
solicitation of proxies to elect its own slate of directors or to approve its
own proposal, without regard to whether consideration of such nominees or
proposals might be harmful or beneficial to the Company and its shareholders. On
the other hand, by requiring advance notice of nominations by shareholders,
these shareholder notice procedures afford the Board an opportunity to consider
the qualifications of the proposed nominees and, to the extent deemed necessary
or desirable by the Board, to inform shareholders about such qualifications. By
requiring advance notice of other proposed business, the shareholder notice
procedures provide a more orderly procedure for conducting annual meetings of
shareholders and, to the extent deemed necessary or desirable by the Board,
provide the Board with an opportunity to inform shareholders, prior to such
meeting, of any business proposed to be conducted at the meeting, together with
any recommendations by the Board or statements as to the Board's position
regarding action to be taken with respect to such business, so that shareholders
can better decide whether to attend the meeting or to grant a proxy regarding
the disposition of any such business.
OHIO GENERAL CORPORATION LAW
Certain provisions of the General Corporation Law of Ohio and of the
Company's Articles and Regulations, summarized in the following paragraphs, may
be considered to have an anti-takeover effect and may delay, deter or prevent a
tender offer, proxy contest or other takeover attempt that a shareholder might
consider to be in such shareholder's best interest, including such an attempt as
might result in payment of a premium over the market price for shares held by
shareholders.
Section 1701.59 of the Ohio General Corporation Law provides that a
director shall not be found to have violated his duties under the Ohio General
Corporation Law unless it is proved by clear and convincing evidence that the
director has not acted in good faith, in a manner he reasonably believes to be
in or not opposed to the best interests of the corporation, or with the care
that an ordinary prudent person in a like position would use under similar
circumstances. Further, such section provides that a director shall be liable in
damages for any action he takes or fails to take as a director only if it is
proved by clear and convincing evidence that his action or failure to act
involved an act or omission undertaken with deliberate intent to cause injury to
the corporation or with reckless disregard for the best interests of the
corporation.
Chapter 1704 of the Ohio General Corporation Law prohibits certain
transactions between a Ohio corporation and an "interested shareholder" Chapter
1704 allows for a corporation to exclude itself from Chapter 1704 by exempting
itself in its articles of incorporation. The Company has not included such an
exemptive provision in the Articles.
EXPERTS
The financial statements of the Company as of December 31, 1995 and
1996 and for each of the three years in the period ended December 31, 1996,
appearing in this Prospectus and the Registration Statement have been audited by
Ernst & Young LLP, independent auditors, as set forth in their report thereon
appearing elsewhere herein and are included in reliance upon such reports given
upon the authority of such firm as experts in accounting and auditing.
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LEGAL MATTERS
The legality of the Shares offered hereby will be passed upon
for the Company by Porter, Wright, Morris & Arthur, 41 South High Street,
Columbus, Ohio 43215.
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INDEX TO FINANCIAL STATEMENTS
NETMED, INC.
Page
----
Report of Independent Auditors ...................................... 33
Balance Sheets at December 31, 1994, 1995, and 1996 ................. 34
Statements of Operations for the Years
ended December 31, 1994, 1995 and 1996
and for the Six Months Ended June 30, 1997 (unaudited) .......... 36
Statements of Cash Flows for the Years
ended December 31, 1994, 1995 and 1996
and for the Six Months Ended June 30, 1997 (unaudited) .......... 37
Statements of Stockholders' Equity for the Years
ended December 31, 1994, 1995 and 1996
and for the Six Months Ended June 30, 1997 (unaudited) .......... 38
Notes to Financial Statements ....................................... 39
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REPORT OF INDEPENDENT AUDITORS
The Board of Directors and Stockholders
NetMed, Inc.
We have audited the accompanying balance sheets of NetMed, Inc. (the Company) as
of December 31, 1995 and 1996, and the related statements of operations,
stockholders' equity and cash flows for each of the three years in the period
ended December 31, 1996. These financial statements are the responsibility of
the Company's management. Our responsibility is to express an opinion on these
financial statements based on our audits.
We conducted our audits in accordance with generally accepted auditing
standards. Those standards require that we plan and perform the audit to obtain
reasonable assurance about whether the financial statements are free of material
misstatement. An audit includes examining, on a test basis, evidence supporting
the amounts and disclosures in the financial statements. An audit also includes
assessing the accounting principles used and significant estimates made by
management, as well as evaluating the overall financial statement presentation.
We believe that our audits provide a reasonable basis for our opinion.
In our opinion, the financial statements referred to above present fairly, in
all material respects, the financial position of the Company at December 31,
1995 and 1996, and the results of its operations and its cash flows for each of
the three years in the period ended December 31, 1996, in conformity with
generally accepted accounting principles.
Columbus, Ohio
March 14, 1997 ERNST & YOUNG LLP
34
37
NETMED, INC.
BALANCE SHEETS
DECEMBER 31 JUNE 30,
1995 1996 1997
----------------------------- -----------
(unaudited)
ASSETS
Current assets
Cash and cash equivalents $ 811,359 $ 142,074 $ 213,948
Accounts receivable 75,993 175,512 319,526
Investment in NSI-available for sale 7,696,296 9,238,503 3,165,138
Note receivable from stockholder 50,000 0 0
Prepaid assets 1,021 28,394 20,766
----------------------------- -----------
Total current assets 8,634,669 9,584,483 3,719,378
Notes receivable-NSI 51,080 21,443 21,443
Investment in partnerships 172,679 0 0
Furniture & Equipment (net of 0
accumulated depreciation) 17,316 28,034 27,620
Deferred taxes 348,670 744,162 628,703
Deposits and other assets 1,330 1,468 6,467
----------------------------- -----------
Total assets $ 9,225,744 $ 10,379,590 $ 4,403,611
============================= ===========
LIABILITIES AND STOCKHOLDERS' EQUITY
Current liabilities:
Accounts payable $ 49,931 $ 97,625 $ 120,365
Accrued expenses 81,630 223,536 294,847
Other liabilities 42,831 29,844 39,490
Loan Payable 0 96,909 140,913
Total current liabilities 174,392 447,914 595,615
----------------------------- -----------
Deferred taxes 2,797,673 2,896,609 628,703
Stockholders' equity:
Common stock no par value, 20,000,000
shares authorized, 6,072,936,
10,940,524, and 10,947,114 issued and
outstanding at December 31, 1995 and
1996, and June 30, 1997 2,562,542 3,881,605 4,012,884
Retained deficit (208,480) (801,302) (1,386,496)
Unrealized gain on available-for-sale
securities net of deferred taxes 3,899,617 3,954,764 552,905
----------------------------- -----------
Total stockholders' equity 6,253,679 7,035,067 3,179,293
----------------------------- -----------
----------------------------- -----------
Total liabilities and stockholders' equity $ 9,225,744 $ 10,379,590 $ 4,403,611
============================= ===========
See accompanying notes.
35
38
NETMED, INC.
STATEMENTS OF OPERATIONS
YEAR ENDED DECEMBER 31, SIX MONTHS ENDED JUNE 30
--------------------------------
1994 1995 1996 1996 1997
--------------------------------------------------------------------------------
(UNAUDITED) (UNAUDITED)
Royalty Revenue $ 24,765 $ 48,000 $ 102,813 $ 27,099 $ 339,608
Operating expenses:
Salaries and benefits 196,825 303,105 838,846 146,733 762,557
Sales and marketing 26,433 74,329 250,389 52,533 376,657
General and administrative 104,103 89,299 240,562 57,741 351,095
Business Development 0 0 85,476 - 59,345
Merger 0 106,416 364,852 134,450 -
----------- ----------- ----------------------------------------------
Total Operating Expenses 327,361 573,149 1,780,125 391,457 1,549,654
----------- ----------- ----------------------------------------------
Operating Loss (302,596) (525,149) (1,677,312) (364,358) (1,210,046)
Other income (expense):
Interest income 19,059 16,606 13,743 10,871 2,099
Interest expense -- (264) (872) -- (4,884)
Gain on sale of available-
for-sale securities -- -- 664,057 -- 745,056
NSI settlement and common
stock transactions -- 1,715,399 -- -- --
Equity income(loss) in
partnerships -- 49,638 (13,451) (4,091) --
----------- ----------- ----------------------------------------------
Total other income 19,059 1,781,379 663,477 6,780 742,271
----------- ----------- ----------------------------------------------
Income(loss) before income tax (283,537) 1,256,230 (1,013,835) (357,578) (467,775)
Income tax (benefit) expense 0 (68,715) (421,013) (122,001) 117,419
----------- ----------- ----------------------------------------------
Net (loss) income $ (283,537) $ 1,324,945 $ (592,822) $ (235,577) $ (585,194)
----------- ---------------------------------------------------------------
Net (loss) income per share $ (0.05) $ 0.21 $ (0.09) $ (0.04) $ (0.05)
=========== =========== ==============================================
Shares used in computation 5,860,336 6,439,594 6,263,924 6,072,936 10,946,316
=========== =========== ==============================================
See accompanying notes.
36
39
NETMED, INC.
STATEMENTS OF CASH FLOWS
SIX MONTHS ENDED
YEAR ENDED DECEMBER 31, JUNE 30,
1994 1995 1996 1996 1997
------------------------------------------------- ----------------------------
(unaudited) (unaudited)
OPERATING ACTIVITIES
Net loss $ (283,537) $ 1,324,945 $(592,822) $ (235,577) $ (585,194)
Adjustments to reconcile net loss to
net cash provided (used in) operating
activities:
Depreciation and amortization 8,152 7,496 7,776 3,000 7,200
Recognition of deferred tax assets - (68,715) (421,013) (122,001) 115,459
Equity (income)/loss in partnership - (49,638) 13,451 4,091 -
Gain on available-for-sale securities - - (664,057) - (745,056)
Gain on settlement and exercise of
warrants with NSI - (1,402,002) - - -
Deferred compensation - - 410,000 - 131,279
Changes in operating assets and liabilities:
Accounts receivable (24,765) (42,548) (55,727) (95,638) (144,014)
Note receivable from stockholder 50,000 - 50,000 - -
Prepaid assets - - (27,373) - 7,628
Deposits and other assets - - - - (4,999)
Accounts payable (23,905) 49,931 47,694 159,741 22,740
Accrued expenses and other
liabilities 15,574 94,127 101,398 (334,453) 81,467
----------- ----------- ---------- ----------------------------
Net cash used in operating activities (358,481) (86,404) (1,130,673) (620,837) (1,113,490)
INVESTING ACTIVITIES
Sale of NSI stock - - 750,057 - 1,148,102
Net cash advances to predecessor companies
in contemplation of Merger - - (400,183) - -
Notes receivable-NSI 70,717 74,961 29,637 29,637 -
Purchase of furniture and equipment (7,200) (4,260) (18,494) - (6,742)
Other assets (172) 1,000 (138) - -
----------- ---------- --------- ----------------------------
Net cash provided by investing
activities 63,345 71,701 360,879 29,637 1,141,360
FINANCING ACTIVITIES
Proceeds from stock subscription
receivable 290,975 - - - -
Issuance of common stock and options
exercised 98,309 290,517 3,600 - -
Proceeds from note payable - - 96,909 - 44,004
----------- ---------- --------- ----------------------------
Net cash provided by financing activities 389,284 290,517 100,509 - 44,004
----------- ---------- --------- ----------------------------
Net increase (decrease) in cash 94,148 275,814 (669,285) (591,200) 71,874
Cash and cash equivalents at beginning
of period 441,397 535,545 811,359 811,359 142,074
----------- ---------- --------- ----------------------------
Cash and cash equivalents
at end of period $ 535,545 $ 811,359 $ 142,074 $ 220,159 $ 213,948
=========== ========== ========= ============================
See accompanying notes.
37
40
NETMED, INC.
STATEMENTS OF STOCKHOLDERS' EQUITY
ADJUSTMENTS
TO UNREALIZED RETAINED
COMMON GAINS EARNINGS
STOCK (LOSSES) (DEFICIT) TOTAL
-------------------------------------------------------------
Balance, January 1, 1994 $ 2,173,716 $ - $(1,249,888) $ 923,828
Stock issued and warrants exercised 98,309 - -- 98,309
Net loss - - (283,537) (283,537)
-------------------------------------------------------------
Balance December 31, 1994 2,272,025 - (1,533,425) 738,600
Stock issued and warrants exercised 290,517 - - 290,517
Adjustment to unrealized gains net
of tax - 3,899,617 - 3,899,617
Net Income - - 1,324,945 1,324,945
-------------------------------------------------------------
Balance, December 31, 1995 2,562,542 3,899,617 (208,480) 6,253,679
Stock options exercised 3,600 - - 3,600
Net assets acquired via merger 905,463 1,765,838 - 2,671,301
Adjustment to unrealized gains net
of tax - (1,710,691) - (1,710,691)
Deferred compensation stock options 410,000 - - 410,000
Net loss - - (592,822) (592,822)
-------------------------------------------------------------
Balance, December 31, 1996 3,881,605 3,954,764 (801,302) 7,035,067
Net Loss (unaudited) - - (585,194) (585,194)
Adjustment to unrealized gains net
of tax (unaudited) - (3,401,859) - (3,401,859)
Deferred compensation stock options
(unaudited) 131,279 - - 131,279
-------------------------------------------------------------
Balance, June 30, 1997 (unaudited) $ 4,012,884 $ 552,905 $(1,386,496) $ 3,179,293
=============================================================
See accompanying notes.
38
41
NETMED, INC.
NOTES TO FINANCIAL STATEMENTS
DECEMBER 31, 1996
1. ORGANIZATION AND BASIS OF PRESENTATION
On December 5, 1996, the Company's shareholders approved an
Agreement and Plan of Merger (the "Merger Agreement") whereby Cytology Indiana,
Inc., Indiana Cytology Review Company, ER Group, Inc., CCWP Partners, Inc.
("CCWP"), and Carolina Cytology, Inc. (the "Predecessor Companies") were merged
with and into the Company (the "Merger"). The Merger was effective on December
16, 1996 and the Company issued, in the aggregate, 4,849,988 shares of its
common stock, without par value, in exchange for the issued and outstanding
shares of the Predecessor Companies. Under terms of the Merger Agreement, the
Company changed its name from Papnet of Ohio, Inc. to NetMed, Inc
Prior to the Merger, Papnet of Ohio, Inc. and each of the Predecessor Companies
(except for CCWP) held long-term territorial license agreements ("License
Agreement") issued by Neuromedical Systems, Inc. (NSI). The License Agreements
provide the right to sell the "PAPNET(R) System" and the "PAPNET(R) Service" as
described below, in Ohio, Kentucky, Missouri, Georgia, North Carolina and the
Standard Metropolitan Area of Chicago. As a result of the Merger, and in
accordance with an agreement with NSI, the individual License Agreements held by
Papnet of Ohio, Inc. and the Predecessor Companies will be exchanged for a
single License Agreement that encompasses the same territories covered by the
individual License Agreements.
NSI, founded in 1988, is a healthcare technology company focused on diagnostic
screening applications to aid in the early detection of certain cancers. NSI's
first and to date only product, the PAPNET(R) System, was approved for
commercial use in the United States by the Food and Drug Administration (the
"FDA") on November 8, 1995. The PAPNET(R) Service permits laboratories to submit
Pap smear slides to one of NSI's central facilities for processing by the
PAPNET(R) System. NSI's objective is to establish the use of its PAPNET(R)
System as the new standard of care in cervical cancer screening.
The Merger of the Company and the Predecessor Companies occurred in connection
with the initial registration of the Company's common stock with the Securities
and Exchange Commission (SEC) which resulted in the public trading of the
Company's common stock. The Merger was accounted for at historical cost based on
the guidance in SEC Staff Accounting Bulletins 48 and 97. The results of
operations of the Predecessor Companies have been combined with those of the
Company on a prospective basis commencing at the date of Merger. The following
displays summarized pro forma results of operations assuming the Merger
transaction occurred on January 1, 1995:
39
42
1. ORGANIZATION AND BASIS OF PRESENTATION (CONTINUED)
Pro Forma
Year ended December 31
1995 1996
---------------------------------
Royalty revenue $ 84,000 $ 222,002
Operating loss (641,788) (2,153,257)
Net (loss) income 2,484,546 (1,032,865)
Net (loss) income per share .23 (.10)
The Company received the following assets and assumed the following liabilities
at the Merger date:
Cash $ 41,000
Accounts receivable 44,000
NSI common stock 4,457,000
----------
Totals assets $4,542,000
Payable to NetMed, Inc. $ 441,000
Accrued liabilities 27,000
Deferred taxes 1,256,000
Minority interest 146,000
----------
1,870,000
==========
Net equity at Merger $2,672,000
==========
The payable to the Company was offset against a related receivable from the
Predecessor Companies recorded on the books of the Company at the date of
Merger. In addition, the minority interest represented Net Med's interest in two
partnerships controlled by certain Predecessor Companies (see Note 2).
2. SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
Use of Estimates
The preparation of financial statements in conformity with generally accepted
accounting principles 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 financial statements.
Estimates also affect the reported amounts of revenues and expenses during the
reporting period. Actual results may differ from these estimates.
Cash Equivalents
The Company considers all short-term deposits and highly liquid investments
purchased with an original maturity of three months or less to be cash
equivalents.
Investment in Partnerships
Prior to the Merger described in Note 1, the Company owned minority interests
in two partnerships which were accounted for by the equity method. The majority
owners of these partnerships were parties to the Merger Agreement, so the
partnerships were merged into the Company at the effective date of the Merger.
Furniture and Equipment
Furniture and equipment consists of office furniture and computer equipment
recorded at cost which is being depreciated on an accelerated method over
estimated useful lives ranging from five to seven years.
40
43
2. SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES (CONTINUED)
License Agreement
The License Agreement expires in 2025, but provides for a 20 year renewal
option. Amounts paid by the Company to NSI in exchange for the License Agreement
have been expensed in the years paid. This accounting reflects the uncertainty
as to the recoverability of amounts paid for the License Agreement, which was
contingent on FDA approval of the PAPNET(R) System and the ability of NSI and
the Company to develop a profitable market for the technology.
Royalty Revenue
Pursuant to the License Agreement, the Company is entitled to receive a
calculated royalty or a specified percentage of NSI's annual slide processing
revenues less certain expenses, up to specific annual monetary limits for each
licensee. Royalty revenue is recognized as earned based on the License
Agreement.
Income Taxes
The Company accounts for income taxes using the liability method under Statement
of Financial Accounting Standards No. 109 "Accounting for Income Taxes."
Deferred items are determined based on differences between the financial
reporting and tax basis of assets and liabilities, and are measured using the
enacted rates and laws that will be in effect when the differences are expected
to reverse.
Stock-Based Compensation
The Company accounts for stock compensation arrangements in accordance with APB
Opinion No. 25, "Accounting for Stock issued to Employees." The pro forma
information regarding net (loss) income and net (loss) income per share as
required by Statement of Financial Accounting Standards No.123, "Accounting for
Stock-Based Compensation" ("SFAS No. 123") is disclosed in "Note 4 - Stock
Options and Warrants."
Reclassification
Certain amounts presented for 1994 and 1995 have been reclassified to conform to
the 1996 presentation.
Net (Loss) Income Per Share
Net (loss) income per share amounts are based on the weighted average common and
common equivalent shares outstanding during the respective periods (including
4,849,988 shares issued in connection with the Merger on December 16, 1996).
Common stock equivalents were antidilutive in 1996 and 1994; therefore, they
were excluded from the calculation of net loss per share.
3. INVESTMENT IN NSI
The Company owns stock in NSI as a result of the exercise of warrants and
settlement of certain claims with NSI. The investment is classified as
available-for-sale and is carried at fair value, with the unrealized gains and
losses, net of tax, reported as a separate component of stockholders' equity.
NSI trades publicly on the NASDAQ NMS under the symbol "NSIX." During 1996, the
Company sold 43,000 shares of NSI stock which resulted in a gain of $664,057
which was reported as other income.
As of December 31, 1996, the Company owned 697,246 shares of NSI stock at a cost
of $2,647,237. The NSI common stock has been recorded in the accompanying
balance sheet based on its $13.25 closing price on December 31, 1996. On March
14, 1997, NSI common stock closed trading at $9.625 per share.
The exercise of the warrants in NSI was completed in 1995 utilizing a cashless
exercise provision in the warrant agreement. This resulted in a gain of
$652,250 which has been reported as other income. As a result of settling
certain claims with NSI in December 1995, the Company received 53,939 shares of
NSI stock resulting in a gain of
41
44
$749,752 which is recorded in other income. In addition, the Company was
allocated the right to purchase 65,000 shares of NSI stock at NSI's initial
public offering. The Company purchased and sold the entire 65,000 shares for
$1,292,363 during 1995 resulting in a realized gain of $313,397 which has been
recorded as other income.
During the six-month period ended June 30, 1997, the Company sold 125,000
shares of NSI stock which resulted in a gain of $745,056 which was reported as
other income. As of June 30, 1997, the Company owned 572,246 shares of NSI
stock at a cost of $2,243,584. The NSI common stock has been recorded in the
accompanying balance sheet based upon its $5.53 closing price on June 30, 1997.
On August 31, 1997, the NSI common stock closed trading at $3.50 per share.
4. STOCK OPTIONS AND WARRANTS
The Company's 1995 Stock Option Plan (the "Stock Option Plan") provides for the
granting of options that may either meet the requirements of Section 422
("Incentive Options") of the Internal Revenue Code, as amended (the "Code") or
not meet such requirements ("Nonqualified Options"). Key employees, officers,
and directors of, and consultants and advisors who render services to, the
Company are eligible to receive options under the Stock Option Plan. The number
of shares available for grants under the Stock Option Plan was 300,000 at
December 31, 1995 and 1996.
Pro forma information regarding net income and earnings per share is required by
SFAS No. 123, which also requires that the information be determined as if the
Company has accounted for its employee stock options granted subsequent to
December 31, 1994 under the fair value method of that Statement. The fair value
for these options was estimated at the date of grant using a Black-Scholes
option pricing model with the following weighted-average assumptions for 1995
and 1996: risk-free interest rate of 6.0%; no dividend yield; volatility factor
of the expected market price of the Company's common stock of .62; and expected
lives ranging from 2 to 5 years.
If the Company had elected to recognize compensation cost based on the fair
value of options at the grant date as prescribed by SFAS No. 123, the following
displays what reported net income (loss) and per share amounts would have been:
Pro Forma Years Ended
December 31,
1995 1996
---------------------------------
Net (loss) income $ 1,257,467 $(873,876)
Net (loss) income per share $ .20 $ (.14)
The pro forma financial effects of applying SFAS No. 123 are not likely to be
representative of the pro forma effects on reported results of operations for
future years.
The following is a summary of the stock option activity for a prior
non-qualified plan (no additional options may be granted under this plan):
42
45
4. STOCK OPTIONS AND WARRANTS (CONTINUED)
Number of Weighted Average
Shares Exercise Price
-------------------------------
Non-Qualified Plan
Outstanding at December 31, 1993 397,600 $ 1.21
Issued 32,000 $ 2.75
Expired 24,000 $ 1.38
---------
Outstanding at December 31, 1994 405,600 $ 1.32
Issued 16,000 $ 11.00
Expired 56,000 $ 1.38
---------
Outstanding at December 31, 1995 365,600 $ 1.74
Issued 56,000 $ 1.55
Exercised 21,200 $ 1.53
Expired 64,000 $ 1.53
---------
Outstanding at December 31, 1996 336,400 $ 1.76
=========
Exercisable at December 31, 1994 197,600 $ 1.22
Exercisable at December 31, 1995 349,600 $ 1.31
Exercisable at December 31, 1996 336,400 $ 1.76
During 1996, the Company extended the expiration date of 56,000 options due to
expire near the end of the year. Accounting Principles Board Opinion No. 25
requires that extended options be treated as if they were a new grant. The
exercise price set for these options was below the market price at the date of
grant and resulted in $410,000 in compensation expense. These options had a
weighted-average fair value and a weighted-average exercise price of $7.60 and
$1.55, respectively. During 1995, the Company issued 16,000 options with an
exercise price equal to the market price at the grant date. The weighted average
fair value of these options was $6.39. Exercise prices for options outstanding
at December 31, 1996 ranged from $1.09 to $11.00 and had a weighted-average
remaining contractual life of 6.57 years.
As of December 31, 1996, there were outstanding 47,020 warrants for the
President of the Company and 24,000 for a former consultant to purchase stock at
exercise prices of $.875 per share and $1.25 per share, respectively.
Number of Weighted Average
Shares Exercise Price
-------------------------------
Outstanding at December 31, 1993 339,040 $ 1.01
Exercised (84,000) $ 1.25
--------
Outstanding at December 31, 1994 255,040 $ .93
Exercised during 1995 (184,020) $ .90
--------
Outstanding at December 31, 1995
and December 31, 1996 71,020 $ 1.25
=======
43
46
5. INCOME TAXES
Significant components of deferred tax assets and liabilities are as follows:
1995 1996
---------------------------------
Loss carryforwards $ 348,670 $ 580,162
Unrealized gains on investments (2,517,718) (2,636,509)
Gain on NSI warrants (260,100) (260,100)
Income from Equity Investee (19,855) -
Stock options issued - 164,000
---------------------------------
Net deferred tax liability $(2,449,003) $(2,152,447)
=================================
At December 31, 1996, the Company had unused NOL carryforwards for tax purposes
of approximately $329,000, $320,000, $211,000, and $251,000 which expire in
2007, 2008, 2009 and 2010, respectively.
At December 31, 1994, a full valuation allowance was recorded due to the lack of
deferred tax liabilities, historical income and tax planning strategies. For
1995 and 1996, due to the existence of a significant deferred tax liability, a
valuation allowance was not required.
The reconciliation of income tax computed at the statutory rate to the recorded
tax provision (benefit) is:
1994 1995 1996
---------------------------------------
Tax provision (benefit) at statutory rate $ (96,402) $ 427,118 $(344,704)
Benefit of state loss carryforward - - (76,309)
Recognition of previously reserved tax
assets - (495,833) -
Valuation allowance provided 96,402 - -
========= ========= =========
Total tax provision (benefit) $ - $ (68,715) $(421,013)
========= ========= =========
6. NOTE RECEIVABLE FROM STOCKHOLDER
On October 14, 1994, the Company loaned one of its officers and stockholders
$50,000, at prime plus 1/2% interest. Under the loan agreement, effective with
the Merger described in Note 1, the loan was deemed a bonus and converted into
compensation during the year ended December 31,1996.
7. LEASES
The Company leases facilities and equipment under operating leases. Commitments
for these leases approximate $21,000 per year through August 14, 2001. Rent
expense for the years ended December 31, 1994, 1995 and 1996 was $15,526,
$19,537 and $41,677, respectively.
8. UNAUDITED FINANCIAL STATEMENTS
The financial statements as of June 30, 1997 and for the six months ended June
30, 1996 and 1997 are unaudited; however, in the opinion of management, all
adjustments (consisting of normal recurring adjustments) necessary for a fair
presentation of the financial statements for these interim periods have been
included. The results for the interim period ended June 30, 1997 are not
necessarily indicative of the results to be obtained for the full fiscal year
ending December 31, 1997.
9. SUBSEQUENT EVENT (UNAUDITED)
On August 13, 1997, the Company issued $3,000,000 in principal amount of 6%
Secured Convertible Subordinated Debentures (the "Debentures") to certain
investors in a private placement. The Debentures are due August 13, 2000, bear
interest at a rate of 6% per annum, and are redeemable by the Company. The
Debentures and any interest accrued thereon may be converted into common stock
of the Company at any time. However, no sales of conversion shares may be made
prior to November 11, 1997, and during the period from November 11, 1997 through
May 10, 1998 (the 91st through 270th day after the closing) the maximum
aggregate number of conversion shares which can be sold is 500,000. After May
10, 1998 (the 270th day after the closing), 100% of the conversion shares may be
sold. The Company can prohibit sales during the period from December 14, 1997 to
February 1, 1998 (the "Blackout Period"). The Debentures are convertible into
shares of the Company's common stock based on the "Conversion Price" at the time
of conversion, which varies based on the date when the Debentures are converted.
For the period through March 31, 1998, the Conversion Price is an amount equal
to 80% of the average closing bid price of the common stock on the American
Stock Exchange for the previous three business days ending on the day before the
conversion date. For the period beginning April 1, 1998, the Conversion Price is
an amount equal to 75% of the average closing bid price of the common stock on
the American Stock Exchange for the previous three business days ending on the
day before the conversion date.
The Debentures are secured by 475,000 shares of common stock of Neuromedical
Systems, Inc. owned by the Company (the "NSI Shares"). If at any time prior to
March 31, 1998, the conversion price is $3.00 or less, the holders of the
Debentures may elect to exercise their conversion rights for NSI Shares, rather
than common stock of the Company, at a 20% discount from the market price at the
time of conversion. If the Company prohibits sales during the Blackout Period,
and the trading volume in the common stock prior to December 15, 1997 does not
meet defined minimums, the holders may convert into the NSI Shares at a discount
from the market price which would produce a 25% return on an annualized basis.
The NSI Shares may be released from the pledge ratably as the outstanding
principal amount of Debentures is reduced.
In connection with this financing, the Company issued warrants to the investors
and to investment bankers. The warrants are exercisable at any time prior to
August 13, 2000 at exercise prices of $7.79 per share (for up to 150,000 Shares)
and $9.35 per share (for up to 65,000 shares).
The Company will incur a one time expense related to the issuance of the
Debentures of approximately $1,100,000 in the quarter ending September 30, 1997.
44
47
================================================================================
NO PERSON HAS BEEN AUTHORIZED TO GIVE ANY INFORMATION OR TO MAKE ANY
REPRESENTATIONS OTHER THAN THOSE CONTAINED IN THIS PROSPECTUS, AND IF GIVEN OR
MADE, SUCH INFORMATION OR REPRESENTATION NOT CONTAINED HEREIN MUST NOT BE RELIED
UPON AS HAVING BEEN AUTHORIZED BY THE COMPANY OR ANY SELLING SHAREHOLDER. THIS
PROSPECTUS DOES NOT CONSTITUTE AN OFFER TO SELL OR THE SOLICITATION OF AN OFFER
TO BUY ANY SECURITIES OTHER THAN THE SECURITIES TO WHICH IT RELATES OR AN OFFER
TO SELL OR THE SOLICITATION OF AN OFFER TO BUY SUCH SECURITIES IN ANY
CIRCUMSTANCES IN WHICH SUCH OFFER OR SOLICITATION IS UNLAWFUL. NEITHER THE
DELIVERY OF THIS PROSPECTUS NOR ANY SALE MADE HEREUNDER SHALL, UNDER ANY
CIRCUMSTANCES, CREATE ANY IMPLICATION THAT THERE HAS BEEN NO CHANGE IN THE
AFFAIRS OF THE COMPANY SINCE THE DATE HEREOF OR THAT THE INFORMATION HEREIN IS
CORRECT AS OF ANY TIME SUBSEQUENT TO ITS DATE.
TABLE OF CONTENTS
Page
----
Available Information....................................... 1
Summary of the Prospectus................................... 2
Risk Factors................................................ 3
Price Range of Common Stock
and Dividend Policy..................................... 7
Use of Proceeds............................................. 8
Selected Financial Data..................................... 8
Management's Discussion and Analysis
of Financial Condition and Results
of Operations........................................... 8
Business.................................................... 12
Management.................................................. 18
Ownership of Common Stock by
Management and Principal Shareholders................... 24
Certain Relationships and
Related Transactions................................... 25
Selling Shareholders........................................ 26
Plan of Distribution........................................ 27
Description of Capital Stock................................ 27
Certain Provisions of Articles
and Regulations......................................... 28
Experts..................................................... 31
Legal Matters............................................... 31
Financial Statements........................................ 32
================================================================================
1,500,000 Shares
NETMED, INC.
COMMON SHARES
(without par value)
September __, 1997
================================================================================
48
PART II
INFORMATION NOT REQUIRED IN PROSPECTUS
ITEM 13. OTHER EXPENSES OF ISSUANCE AND DISTRIBUTION
The expenses relating to the registration of the Shares of Common Stock
being offered hereby, other than underwriting discounts and commissions, will be
borne by the Company. Such expenses are estimated to be as follows:
Item Amount
---- ------
Securities and Exchange Commission
Registration Fee $21,656.25
----------
Legal Fees and Expenses 2,500
Accounting Fees and Expenses 5,000
Miscellaneous Expenses 7,000
----------
Total $ 36,156
----------
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ITEM 14. INDEMNIFICATION OF DIRECTORS AND OFFICERS.
As permitted by the Ohio General Corporation Law, Article NINTH of
the Registrant's Amended and Restated Articles of Incorporation ("Articles")
provides that a director, officer, incorporator, or any former officer or
director of the Registrant shall be indemnified by the Registrant to the fullest
extent permitted by the Ohio General Corporation Law.
Indemnification of directors, officers, employees and agents is
required under Section 1701.13 of the Ohio General Corporation Law in those
cases where the person to be indemnified has been successful on the merits or
otherwise in defense of a lawsuit. Indemnification is permitted in third party
actions where the indemnified person acted in good faith and in a manner he
reasonably believed to be in or not opposed to the best interests of the
corporation and in criminal actions where he had no reasonable cause to believe
his conduct was unlawful. Indemnification is also permitted in lawsuits brought
by or on behalf of the corporation if the standards of conduct described above
are met, except that no indemnification is permitted in respect to any matter in
which the person is adjudged to be liable for negligence or misconduct in the
performance of his duty to the corporation unless a court shall determine that
indemnification is fair and reasonable in view of all the circumstances of the
case. In cases where indemnification is permissive, a determination as to
whether the person met the applicable standard of conduct must be made either by
the court, disinterested directors, by independent legal counsel, or by the
shareholders. Such indemnification rights are specifically not deemed to be
exclusive of other rights of indemnification by agreement or otherwise and the
corporation is authorized to advance expenses incurred prior to the final
disposition of a matter upon receipt of an undertaking to repay such amounts on
a determination that indemnification was not permitted in the circumstances of
the case.
Under Section 1701.13 of the Ohio General Corporation Law, a
corporation may purchase and maintain insurance on behalf of any person who is
or was a director, officer, employee, or agent of the corporation, or who, while
serving in such capacity, is or was at the request of the corporation, a
director, officer, employee or agent of another corporation or legal entity or
of an employee benefit plan, against liability asserted against or incurred by
such person in any such capacity whether or not the corporation would have the
power to provide indemnity under Section 1701.13 of the Ohio General Corporation
Law. The Registrant has not applied for directors' and officers' liability
insurance.
The above discussion of the Registrant's Articles and of Section
1701.13 of the Ohio General Corporation Law is not intended to be exhaustive and
is respectively qualified in its entirety by such Articles of Incorporation and
statute.
ITEM 15. RECENT SALES OF UNREGISTERED SECURITIES.
In October and December, 1994, the Company issued 21,000 common
shares, without par value, to Corna Securities, Inc., upon the exercise of
warrants with an exercise price of $5.00 per share, with total proceeds of
$105,000. The transaction was exempt from registration under Sections 4(2) and
4(6) of the Securities Act, and Rule 506 of Regulation D.
On April 21, 1995, the Company issued 19,800 common shares, without
par value, to David J. Richards, President of the Company, upon the exercise of
a stock option for 22,000 shares with an exercise price of $3.50 per share. The
options were fully exercised, but due to the option holder's election of a
cashless exercise feature of the options, the net number of shares issued was
19,800. The transaction was exempt from registration under Sections 3(b), 4(2)
and 4(6) of the Securities Act, and Rules 504 and 506 of Regulation D.
On June 9, 1995, the Company issued 6,980 common shares, without par
value, to David J. Richards, President of the Company, upon the exercise of a
stock option for 7,580 shares with an exercise price of $1.75 per share. The
options were fully exercised, but due to the option holder's election of a
cashless exercise feature of the options, the net number of shares issued was
6,980. The transaction was exempt from registration under Sections 3(b), 4(2)
and 4(6) of the Securities Act, and Rules 504 and 506 of Regulation D.
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On August 9, 1995, the Company issued 32,502 common shares, without
par value, to David J. Richards, President of the Company, upon the exercise of
a stock option for 34,430 shares with an exercise price of $1.75 per share. The
options were fully exercised, but due to the option holder's election of a
cashless exercise feature of the options, the net number of shares issued was
32,502. The transaction was exempt from registration under Sections 3(b), 4(2)
and 4(6) of the Securities Act, and Rules 504 and 506 of Regulation D.
On October 20, 1995, the Company sold 18,000 common shares, without
par value, to 25 persons in a public offering exempt from registration under
Rule 504 of Regulation D, which was registered by description in Ohio pursuant
to Section 1707.06(A)(2), Ohio Rev. Code. The underwriter for the offering was
Corna Securities, Inc. Gross proceeds of the offering were $330,112.50, and the
total underwriting commission was $33,112.50.
On September 25, 1996, the Company issued 14,000 common shares,
without par value, to Jeffrey Guest, a former employee of the Company, upon the
exercise of a stock option for 17,600 shares with an exercise price of $1.38 per
share. The options were fully exercised, but due to the option holder's election
of a cashless exercise feature of the options, the net number of shares issued
was 14,000. The transaction was exempt from registration under Sections 3(b) and
4(2) of the Securities Act, and Rules 504 and 506 of Regulation D.
On January 23, 1997, the Company issued 3,307 common shares, without
par value, to Melissa Place, a former employee of the Company, upon the exercise
of a stock option for 4,000 shares with an exercise price of $1.37 per share.
The options were fully exercised, but due to the option holder's election of a
cashless exercise feature of the options, the net number of shares issued was
3,307. The transaction was exempt from registration under Sections 3(b) and 4(2)
of the Securities Act, and Rules 504 and 506 of Regulation D.
On October 25, 1996, November 14, 1996, and February 19, 1997, the
Company issued a total of 4,883 common shares, without par value, to the
partners of BRP Ventures Partnership, upon the exercise of a stock option for
8,000 shares with an exercise price of $2.25 per share. The options were fully
exercised, but due to the option holders' election of a cashless exercise
feature for all but 1,600 of the options, the net number of shares issued was
6,320, and the net proceeds to the Company were $3,600. The transaction was
exempt from registration under Sections 3(b) and 4(2) of the Securities Act, and
Rules 504 and 506 of Regulation D.
ITEM 16. EXHIBITS AND FINANCIAL STATEMENT SCHEDULES.
(a) EXHIBITS
EXHIBIT EXHIBIT
NUMBER DESCRIPTION
------ -----------
3.1 Amended and Restated Articles of Incorporation of the
Registrant. (Previously filed as Appendix A to the
Registration Statement on Form S-4, Registration No.
333-8199, and incorporated herein by reference.)
3.2 Amended and Restated Regulations of the Registrant.
(Previously filed as Appendix A to the Registration
Statement on Form S-4, Registration No. 333-8199, and
incorporated herein by reference.)
3.3 Form of Specimen Stock Certificate. (Previously filed as
Exhibit 3(e) to the Registration Statement on Form S-4,
Registration No. 333-8199, and incorporated herein by
reference.)
4.1 Articles FOURTH, SIXTH, SEVENTH, EIGHTH, TENTH, and
ELEVENTH, of the Registrant's Amended and Restated Articles
of Incorporation and Articles I, V and VII of the
Registrant's Amended and Restated Regulations. (Previously
filed as Exhibit 4(b) to the Registration Statement on Form
S-4, Registration No. 333-8199, and incorporated herein by
reference.)
5 * Opinion of Porter, Wright, Moris & Arthur regarding
legality.
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10.1 Settlement Agreement among Neuromedical Systems, Inc. and
the Registrant, Cytology Indiana, Inc., Indiana Cytology
Review Company, ER Group, Inc., Cytology West, Inc.,
Carolina Cytology Licensing Company, Papnet Utah, Inc.,
Carolina Cytology Warrant Partnership, and GRK Partners,
dated as of December 5, 1995. (Previously filed as Exhibit
10(a) to the Registration Statement on Form S-4,
Registration No. 333-8199, and incorporated herein by
reference.)
10.2 Voting Agreement among the Registrant, Cytology Indiana,
Inc., Indiana Cytology Review Company, ER Group, Inc., CCWP
Partners, Inc., and Carolina Cytology, Inc., and certain
shareholders of these entities dated July 5, 1996.
(Previously filed as Exhibit 10(c) to the Registration
Statement on Form S-4, Registration No. 333-8199, and
incorporated herein by reference.)
10.3 Loan Agreement among the Registrant, Cytology Indiana, Inc.,
Indiana Cytology Review Company, ER Group, Inc., CCWP
Partners, Inc., and Carolina Cytology, Inc., dated July 5,
1996, and the Side letter thereof, dated July 18, 1996.
(Previously filed as Exhibit 10(d) to the Registration
Statement on Form S-4, Registration No. 333-8199, and
incorporated herein by reference.)
10.4 Loan Agreement between the Registrant and Cytology West,
Inc. and Papnet Utah, Inc.,dated March 14, 1996. (Previously
filed as Exhibit 10(e) to the Registration Statement on Form
S-4, Registration No. 333-8199, and incorporated herein by
reference.)
10.5 Promissory Note and Security Agreement among Cytology West,
Inc. and the Registrant dated April 5, 1996 and April 4,
1996, respectively. (Previously filed as Exhibit 10(f) to
the Registration Statement on Form S-4, Registration No.
333-8199, and incorporated herein by reference.)
10.6 Guaranty executed by Carl Genberg, guaranteeing all
obligation of Cytology West, Inc., dated April 4, 1996.
(Previously filed as Exhibit 10(g) to the Registration
Statement on Form S-4, Registration No. 333-8199, and
incorporated herein by reference.)
10.7 Security Agreement granting a security interest in
Neuromedical Systems, Inc. stock to the Registrant, executed
by Carl Genberg on April 4, 1996. (Previously filed as
Exhibit 10(h) to the Registration Statement on Form S-4,
Registration No. 333-8199, and incorporated herein by
reference.)
10.8 Amended and Restated 1995 Stock Option Plan of the
Registrant. (Previously filed as Exhibit 10(i) to the
Registration Statement on Form S-4, Registration No.
333-8199, and incorporated herein by reference.)
10.9 * Net Lease between Muirfield Square, Ltd. as Lessor and
Registrant as Lessee, dated September 15, 1997.
10.10 Investment Agreement among the Registrant, CeramPhysics,
Inc. and Ceram Oxygen Technologies, Inc., dated February 28,
1997. (Previously filed as Exhibit 10(j) to Registrant's
1996 Annual Report on Form 10-K, Commission file no.
1-12529, and incorporated herein by reference.)
10.11 Revolving Loan-Grid Note, between the Registrant as the
lender and Ceram Oxygen Technologies, Inc. as maker, dated
February 28, 1997. (Previously filed as Exhibit 10(k) to
Registrant's 1996 Annual Report on Form 10-K, Commission
file no. 1-12529, and incorporated herein by reference.)
10.12 Marketing Support Agreement among Neuromedical Systems,
Inc., NetMed, Inc., and Blue Cross and Blue Shield Mutual of
Ohio, dated January 30, 1997. (Previously filed as
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Exhibit 10(l) to Registrant's 1996 Annual Report on Form
10-K, and incorporated herein by reference.)
10.13 Employment Agreement between the Registrant and David J.
Richards, dated as of April 1, 1997. (Previously filed as
Exhibit 10(a) to Registrant's Quarterly Report on Form 10-Q
for the quarter ending June 30, 1997, and incorporated
herein by reference.)
10.14 * Employment Agreement between the Registrant and William J.
Kelly, Jr., dated as of July 1, 1997.
23 * Consent of Ernst & Young, LLP.
24 * Powers of Attorney.
99.1 * 6% Secured Convertible Subordinated Debenture Purchase
Agreement, dated August 12, 1997, between the Registrant and
CPR (USA), Inc.
99.2 * Pledge Agreement, dated August 12, 1997, among the
Registrant, CPR (USA), Inc., LibertyView Fund LLC,
LibertyView Plus Fund, and National City Bank.
99.3 * Convertible Debenture Escrow Agreement, dated August 12,
1997, among the Registrant, CPR (USA), Inc., and Sheldon E.
Goldstein, P.C.
99.4 * Registration Rights Agreement, dated August 12, 1997,
between the Registrant and CPR (USA), Inc.
99.5 * Debenture, dated August 13, 1997, issued by the Registrant
to CPR (USA), Inc.
99.6 * Warrant to Purchase 73,334 Shares of Common Stock, dated
August 13, 1997, issued by the Registrant to CPR (USA), Inc.
99.7 * Amendment to Convertible Debenture Purchase Agreement.
* Filed with this Registration Statement.
(b) FINANCIAL STATEMENT SCHEDULES
Schedules not listed above are omitted because of the absence of the
conditions under which they are required or because the required information is
included in the financial statements or the notes thereto.
ITEM 17. UNDERTAKINGS.
(a) Insofar as indemnification for liabilities arising under the
Securities Act of 1933 may be permitted to directors, officers and controlling
persons of the registrant pursuant to the foregoing provisions, or otherwise,
the registrant has been advised that in the opinion of the Securities and
Exchange Commission such indemnification is against public policy as expressed
in the Act and is, therefore, unenforceable. In the event that a claim for
indemnification against such liabilities (other than the payment by the
registrant of expenses incurred or paid by a director, officer or controlling
person of the registrant in the successful defense of any action, suit or
proceeding) is asserted by such director, officer or controlling person in
connection with the securities being registered, the registrant will, unless in
the opinion of its counsel the matter has been settled by controlling precedent,
submit to a
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court of appropriate jurisdiction the question whether such indemnification by
it is against public policy as expressed in the Act and will be governed by the
final adjudication of such issue.
(b) The undersigned registrant hereby undertakes that:
(1) For purposes of determining any liability under the Securities
Act of 1933, the information omitted from the form of prospectus filed as part
of this registration statement in reliance upon Rule 430A and contained in a
form of prospectus filed by the registrant pursuant to Rule 424(b)(1) or (4) or
497(h) under the Securities Act shall be deemed to be part of this registration
statement as of the time it was declared effective.
(2) For the purpose of determining any liability under the
Securities Act of 1933, each post-effective amendment that contains a form of
prospectus shall be deemed to be a new registration statement relating to the
securities offered therein, and the offering of such securities at that time
shall be deemed to be the initial bona fide offering thereof.
(3) It will file, during any period in which offers or sales are
being made, a post-effective amendment to this registration statement:
(i) To include any prospectus required by section
10(a)(3) of the Securities Act of 1933;
(ii) To reflect in the prospectus any facts or events
arising after the effective date of the registration statement (or
the most recent post-effective amendment thereof) which,
individually or in the aggregate, represent a fundamental change in
the information set forth in the registration statement.
Notwithstanding the foregoing, any increase or decrease in volume of
securities offered (if the total dollar value of securities offered
would not exceed that which was registered)and any deviation from
the low or high end of the estimated maximum offering range may be
reflected in the form of prospectus filed with the Securities and
Exchange Commission pursuant to Rule 424(b) if, in the aggregate,
the changes in volume and price represent no more than a 20 percent
change in the maximum aggregate offering price set forth in the
"Calculation of Registration Fee" table in the effective
registration statement;
(iii) To include any material information with respect
to the plan of distribution not previously disclosed in the
registration statement or any material change to such information in
the registration statement.
(4) It will remove from registration by means of a post-effective
amendment any of the securities being registered that remain unsold at the
termination of the offering.
SIGNATURES
Pursuant to the requirements of the Securities Act of 1933, as
amended, the Registrant has duly caused this Registration Statement to be signed
on its behalf by the undersigned, thereunto duly authorized, in the City of
Dublin, State of Ohio, on September 15, 1997.
NETMED, INC.
By: /s/ David J. Richards
---------------------------
David J. Richards, President
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Pursuant to the requirements of the Securities Act of 1933, this
registration statement has been signed by the following persons in the
capacities and on the dates indicated:
SIGNATURE TITLE DATE
--------- ----- ----
/s/ David J. Richards President, Director ) September 15, 1997
- -------------------------- (Principal Executive Officer) )
David J. Richards )
)
)
*Kenneth B. Leachman Executive Vice President-Finance, ) September 15, 1997
- -------------------------- (Principal Accounting Officer) )
Kenneth B. Leachman )
)
*John P. Kennedy Vice President-Business Development, ) September 15, 1997
- -------------------------- Treasurer, Asst. Secretary, Director )
John P. Kennedy )
)
*S. Trevor Ferger Director ) September 15, 1997
- -------------------------- )
S. Trevor Ferger )
)
*Cecil J. Petitti Director ) September 15, 1997
- -------------------------- )
Cecil J. Petitti )
)
*Michael S. Blue Director ) September 15, 1997
- -------------------------- )
Michael S. Blue )
)
*By: /s/ David J. Richards
- ---------------------------
Attorney-in-fact for each of the persons indicated
8