-----BEGIN PRIVACY-ENHANCED MESSAGE----- Proc-Type: 2001,MIC-CLEAR Originator-Name: webmaster@www.sec.gov Originator-Key-Asymmetric: MFgwCgYEVQgBAQICAf8DSgAwRwJAW2sNKK9AVtBzYZmr6aGjlWyK3XmZv3dTINen TWSM7vrzLADbmYQaionwg5sDW3P6oaM5D3tdezXMm7z1T+B+twIDAQAB MIC-Info: RSA-MD5,RSA, E2SGfUdmwo48B2jEvntYSzqFIkcBDGDi1eCtxFdo/E6R9gOIEM5+nGATB4XrRcy7 gyK9i9cnhAvrCqsUq5PkSg== 0001017813-98-000002.txt : 19980401 0001017813-98-000002.hdr.sgml : 19980401 ACCESSION NUMBER: 0001017813-98-000002 CONFORMED SUBMISSION TYPE: 10-K PUBLIC DOCUMENT COUNT: 3 CONFORMED PERIOD OF REPORT: 19971231 FILED AS OF DATE: 19980331 SROS: NASD FILER: COMPANY DATA: COMPANY CONFORMED NAME: PATIENT INFOSYSTEMS INC CENTRAL INDEX KEY: 0001017813 STANDARD INDUSTRIAL CLASSIFICATION: SERVICES-MISC HEALTH & ALLIED SERVICES, NEC [8090] IRS NUMBER: 161476509 STATE OF INCORPORATION: DE FISCAL YEAR END: 1231 FILING VALUES: FORM TYPE: 10-K SEC ACT: SEC FILE NUMBER: 000-22319 FILM NUMBER: 98583481 BUSINESS ADDRESS: STREET 1: 46 PRINCE ST CITY: ROCHESTER STATE: NY ZIP: 14607 BUSINESS PHONE: 7162427200 MAIL ADDRESS: STREET 1: 46 PRINCE ST CITY: ROCHESTER STATE: NY ZIP: 14607 10-K 1 FORM 10-K FORM 10-K. - ANNUAL REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 (Mark One) [ X ] Annual Report Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934 For the fiscal year ended December 31, 1997 or [ ] Transition Report Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934 For the transition period from to Commission file number 333-07643 PATIENT INFOSYSTEMS, INC. (Exact name of registrant as specified in its charter) Delaware 16-1476509 (State or other jurisdiction of (I.R.S. Employer Identification No.) incorporation or organization) 46 Prince Street, Rochester, NY 14607 (Address of principal executive offices) (Zip Code Registrant's telephone number, including area code (716) 242-7200 Securities registered pursuant to Section 12(b) of the Act: Title of each class registered Name of each exchange on which registered None Securities registered pursuantto Section 12(g) of the Act: Common Stock, $.01 Par Value Per Share (Title of Class) Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days. Yes No Indicate by check mark if disclosure of delinquent filers pursuant to Item 405 of Regulation S-K ((delta)229.405 of this chapter) is not contained herein, and will not be contained, to the best of the registrant's knowledge, in definitive proxy or information statements incorporated by reference in Part III of this Form 10-K or any amendment to this Form 10-K. [X] As of February 28, 1998, 8,012,842 shares of common stock were outstanding, and the aggregate market value of the common shares of Patient Infosystems, Inc. held by non-affiliates was approximately $15 million. DOCUMENTS INCORPORATED BY REFERENCE Portions of the Proxy Statement for the Registrant's 1998 Annual Meeting of Stockholders to be filed prior to April 30, 1998 are incorporated by reference in Part III. PART I Item 1. Description of Business. General Patient Infosystems, Inc. (the "Company" or "Patient Infosystems") was incorporated in the State of Delaware on February 22, 1995 under the name DSMI Corp., changed its name to Disease State Management, Inc. on October 13, 1995, and then changed its name to Patient Infosystems, Inc. on June 28, 1996. The Company's principal executive offices are located at 46 Prince Street, Rochester, New York 14607 and its telephone number is 716-242-7200. Patient Infosystems provides patient-centered health care information systems and services to manage, collect and analyze information to improve patient compliance with prescribed treatment protocols, to improve the process of off-site patient management and to enhance patient and provider information. The Company's technology platform integrates an advanced voice recognition telephone system, high speed data processing and analysis capability, and demand publishing and information distribution capabilities. The system utilizes trained telephone operators and computerized interactive voice response technology and behavior modification based treatment to communicate via telephone directly with the patient at home in order to gather relevant patient data. This data is subsequently evaluated and automatically transmitted via computer generated reports to health care payors, providers and patients, with these reports being tailored to the specific needs of each recipient. The Company markets its services to pharmaceutical manufacturers, pharmacy benefit managers ("PBMs") and health care payors, such as managed care organizations ("MCOs") and insurance companies and health care providers, to collect data outside of the physician office and institutional setting to enhance compliance by patients with prescribed treatment protocols. The Company`s systems may also be used to address the full spectrum of health care information needs with respect to care quality, patient satisfaction and patient and provider education. During its first two years of operations, the Company has emphasized the development of disease management programs, which accounted for a substantial portion of its revenue during 1997. However, during 1997, the Company devoted increased resources to the development of other applications of its technology platform, including demand management, patient surveys and outcomes analysis. Information Capture, Delivery and Analysis Technologies The Company's technology platform integrates an advanced voice recognition telephone system, high speed data processing and analysis capability, demand publishing and information distribution capabilities and behavior modification based compliance algorithms. The system utilizes trained telephone operators and computerized interactive voice response technology to communicate via telephone directly with the patient at home in order to gather relevant patient data. In order to minimize costly live operator interaction, a computer initiates each call to the patient, which call is automatically transferred to an operator and finally routed to an automated speech application. Patients respond to the recorded speech application by speaking normally. This approach is designed to enable a wider variety of possible responses than is achievable via telephone key pad. Depending on the patient's response, situation-specific algorithms are applied to modify future questions and thus help customize the collection of data. The Company's system analyzes and prepares the captured data for automatic delivery to the payor, provider and patient using demand publishing. Demand publishing technology enables the creation of highly individualized reports by inserting stored graphic images and text which can be customized for race, gender and age. These reports are also customized to the patient's specific situation, and the system utilizes the information received during contacts with the patient to further customize the content of the report. The data relevant to the separate report for health care providers is formatted in a customized report to be automatically transmitted via mail, fax or on-line. Each contact with a patient contributes to the establishment of a longitudinal data base which can be analyzed to provide information about treatment modalities for patients, providers and payors. The Company's system is designed to analyze patient compliance to prescribed treatment regimens and gather additional clinical information so that improvements in such regimens can be developed. Integrated Disease State Management System The Company's first application of its integrated information capture and delivery technology is its integrated disease state management system. This system is designed to provide caregivers with the ability to monitor, on a cost-effective basis, patient condition and behavior while the patient is between physician consultations. The Company believes that this will permit caregivers to improve patient compliance and, as a consequence, improve patient outcomes. The Company's disease state management system has three primary components. First, using a panel of recognized medical and clinical experts, the Company develops a disease-specific patient intervention and compliance program that includes a template for the integration of each patient's history, current medical status and treatment protocol. If the program is being developed on a custom basis for a particular customer, the program is developed in consultation with the customer's clinical staff and consultants. Second, the Company establishes periodic telephone contacts with each patient to monitor the patient's compliance with prescribed therapies as well as the patient's treatment progress. Third, using the information obtained from patient contacts and other available information regarding the patient and his or her treatment, such as physician records and pharmacy information, personalized reports are prepared, typically following each patient contact, for evaluation by the patient, the patient's health care provider and, on a periodic basis, payors. Development of Disease-Specific Protocols The Company's disease-specific compliance programs are developed for targeted diseases either on a customized or standardized basis. The Company retains an internal clinical staff and panels of independent medical and clinical experts to identify guidelines of generally accepted treatment protocols and diagnostic interventions for particular diseases. These guidelines serve as a template for information to be gathered from each patient. If the program is being developed on a custom basis for a particular customer, the program is developed in consultation with the customer's clinical staff and consultants. In addition, the Company's internal clinical staff conducts research of available databases and gathers information provided by medical experts, insurance providers, governmental agencies, Medicare and Medicaid and other sources to develop with the medical experts the disease-specific program structure. The resulting compliance protocols are designed to enable the Company to gather the necessary patient information to determine the extent of a patient's compliance with his or her prescribed treatment, the effectiveness of treatment and the progress of the patient's disease. As the Company's database of disease-specific treatments expands, the Company intends to use that data to modify, update and enhance its own disease state management compliance programs and assist health care providers in improving treatment protocols. Patient Enrollment When a patient is enrolled in one of the Company's disease state management programs a patient history is obtained, including the histories of the chronic illness, medications, and surgical procedures as well as other information deemed relevant by the disease-specific compliance program. This information is included in the Company's database for each patient and is used to create customized reports for distribution to each of the patient's health care provider and payor as well as the patient. The patient report can include information on the prescribed treatment of the patient's disease as well as the use of the program and social support services to improve compliance with the patient's treatment regimen. In addition, the Company's demand publishing technology provides personalized behavior modification and educational materials for the patient. The health care provider report contains the relevant clinical and behavioral information gathered from the patient. The Company has found patient enrollment to be one of the particularly challenging components to establishing effective programs. Although the Company has completed the development of several disease management programs, the Company's customers have been able to provide only limited patients to enroll in the programs. To the extent that the Company's revenue is dependent upon the number of contacts it is able to achieve, it will be required to work closely with its customers to develop methods to increase patient enrollment. Patient Contacts In accordance with a designated patient contact schedule, a patient will periodically receive telephone calls from a live operator who, after confirming the identity of the patient, will transfer the patient to an automated system that will ask specific questions determined in accordance with the disease-specific compliance program and provide information and motivational feedback. Patient contact schedules are established for each disease state management program, with the frequency of patient contact varying with the disease under management and the goal of the applicable treatment and occurring as often as daily or as infrequently as on a quarterly basis. The data gathered from the patient during each contact is processed and stored in the Company's database. The compliance program takes into account patient responses to treatment follow-up questions and initiates specific courses of action which can include positive reinforcement messages, confirmation of prescription instructions and scheduled callbacks to remind the patient of the need to take prescribed medication. In addition, questions to be asked in future calls are modified based upon the patient's responses during previous calls. The Company's disease state management system captures and processes the information obtained from the patient during the contact and integrates this information with the other data maintained by the Company, including prior patient responses, patient medical history, treatments administered to date and the mandated treatment protocols for the disease. This system automatically prepares distinct reports using the Company's demand publishing technologies for the patient and for the physician or other caregiver. Each report is tailored for the particular requirements of each recipient. The patient's report, for example, may include pictures, diagrams and informative discussions relating to the treatment course intended to modify or reinforce certain behaviors. The physician's report would likely be more factual and direct and summarize the clinical and behavioral information that has been gathered. On a periodic basis the Company will provide data to the patient's health care payor with respect to that patient's progress. The Company will be able to include information from various data sources in these reports for the purpose of providing additional information with respect to a patient. For example, the Company may be able to interact with the pharmacy services division of a payor to determine the renewal frequency of prescriptions, which provides an indication of whether a patient is taking his or her medication. In addition, the system provides the flexibility to allow other information from physicians' reports and hospital tests to be included in the periodic reports. Compliance Assistance The Company assists payors and health care providers in monitoring patient compliance and works with health care providers to develop compliance and education programs that can be implemented through the Company's system. The Company's publishing technology enables production of patient-specific compliance and education literature that is customized for an individual patient. Once this literature is prepared it may be delivered to a patient by mail, facsimile or on-line. In addition, the Company can implement a variety of procedures including medication reminders via wireless two-way communication and more frequent telephone communications for non-compliant patients or patients with more difficult treatment regimens. The Company can provide additional support services, such as an 800 number that will provide recorded information with respect to a variety of patient education topics or other support messages. Patient Infosystems Programs The Company is developing customized disease state management and risk assessment programs in conjunction with a number of customers, as well as standardized disease state management programs in the areas of asthma and diabetes. Each of the Company's customer agreements for its customized programs provide for development fees to be paid to the Company upon the achievement of certain milestones. In addition, the agreements for customized disease state management programs all provide for some form of exclusivity period, during which the Company is prohibited from engaging or participating in other projects involving the specific disease target that is the subject of that program. The exclusivity periods extend until, in general, a certain date or certain period (ranging from eight to 24 months) following the achievement of a specified milestone in the development or implementation of the program. The Company enrolled its first patients in a disease state management program in October 1996, and has only a limited number of persons enrolled to date. All of the Company's customer agreements, which are typically terminable without cause by either party, require payment to the Company of operational fees per enrolled patient. The amount of the per patient program operational fee varies with the length, complexity and frequency of patient contacts as dictated by the respective program protocols. Patient enrollment in each of the Company's programs will depend upon the identification and referral by the Company's customers of patients to the Company's system which will vary from program to program. The Company has developed or is developing programs in the following areas: Asthma The Company has completed the development of a disease state management program for asthmatic patients that has been marketed to payors and other participants in the health care industry, and such program has been provided to patients since January 1997. Through February 1998, the Company has had approximately 2,900 interventions with patients participating in these programs. American HomePatient, Inc. ("American HomePatient"), Centra Healthcare Adminstrative Services, Inc. ("Centra"), Harris Methodist Health Plan ("Harris Methodist") and Health Alliance, a Division of Astra Pharma Inc. ("Health Alliance") have retained the Company to provide disease state management programs for patients who are suffering from asthma and are enrolled in health care programs for which these companies provide services. Congestive Heart Failure The Company has a services agreement with Bristol-Myers to develop, implement and operate a disease state management program to aid in the treatment of patients suffering from congestive heart failure. The Company has completed the development of the program in congestive heart failure in the English language, and is currently developing the program in the Spanish language. This program has been provided to patients since April 1997, and through February 1998, the Company has had approximately 6,000 interventions with patients participating in this program. Diabetes The Company has completed the development of a disease state management program for diabetic patients that has been marketed to payors and other participants in the health care industry. Bristol-Myers, Centra and Health Resources have retained the Company to provide this disease state management program for patients who are suffering from diabetes and are enrolled in health care programs for which these companies provide services. These programs have been provided to patients since August of 1997, and through February 1998, the Company has had approximately 760 interventions with patients participating in these programs. Secondary Cardiovascular Disease The Company has entered into a services agreement with Bristol-Myers to develop, implement and operate a disease state management program relating to the prevention of cardiovascular sequelae in patients who have recently experienced certain cardiovascular illnesses or treatments such as angina, cardiac bypass surgery or myocardial infarction. The Company has completed the development of this program in the English language and is continuing to develop the program in the Spanish language. This program has been provided to patients since January 1997, and through February 1998, the Company has had 30 interventions with patients participating in this program. Additional Disease Targets The Company has identified additional opportunities in large chronic disease markets, including in the treatment of hypertension, chronic obstructive pulmonary disease, depression, cancer, osteoporosis, arthritis, HIV infection and high risk pregnancy. Each of these targets has been identified as having characteristics which make them attractive candidates for the Company's programs. The Company is currently involved in discussions with customers for the development of programs in a variety of these areas. Significant Customer Concentration The Company's current contracts are concentrated in a small number of customers, with several of the Company's most significant contracts being with Bristol-Myers. The Company expects that its sales of services will be concentrated in a small number of customers for the foreseeable future. Consequently, the loss of any one of its customers could have a material adverse effect on the Company and its operations. There can be no assurance that customers will maintain their agreements with the Company, enroll a sufficient number of patients in the programs developed by the Company for the Company to achieve or maintain profitability, or that customers will renew their contracts upon expiration or on terms favorable to the Company. Relationship with Bristol-Myers The Company has entered into several service agreements with Bristol-Myers relating to the development, implementation and operation by the Company of disease state management programs for certain specified diseases, and the development and operation of a patient satisfaction survey and a general medication compliance program (collectively the "Service Agreements"). Each of the Service Agreements provides for an exclusivity period (the "Exclusivity Period"), during which time the Company is prohibited from engaging or participating in any other projects involving the specific disease target that is the subject of the Service Agreements. The Exclusivity Periods extend from the effective dates of the Service Agreements until, in general, a certain date or a certain period (ranging from eight to 24 months) following the achievement of a specified milestone in the development or implementation of the program (such as the completion of the pilot program). Three of the Service Agreements provide that upon conclusion of the Exclusitivity Period, Bristol-Myers has the right to negotiate with the Company for an exclusive arrangement for the administration of the disease state management program, provided that Bristol-Myers has enrolled a certain number of patients in the program to date. The Company is currently involved in discussions relating to the continuation of these programs. In the event that such negotiations prove unsuccessful, Bristol-Myers retains a right of first refusal with respect to any other offers made to the Company for such arrangements for a period of nine or 12 months following the Exclusivity Period. The Service Agreements generally provide that Bristol-Myers retains ownership to certain materials and other work product created by the Company pursuant to the Service Agreements and that the Company is entitled to use other materials and data. The extent of these rights varies by agreement. The Company and Bristol-Myers have agreed to indemnify each other with respect to losses arising from willful or negligent acts or omissions or breaches of the Service Agreements by the indemnifying party pursuant to the Service Agreement. The Service Agreements are terminable without cause by either party with either 30 or 90 days' notice. The Company has entered into Service Agreements with Bristol-Myers in the disease areas of congestive heart failure, secondary cardiovascular disease, chronic pain and weight management, diabetes and hypertension compliance program. Other Applications of the Integrated Information Capture and Delivery Technology Demand Management Demand management involves assisting providers in evaluating patient treatment needs to identify those patients who may not require immediate or intensive services. The goal of demand management is to reduce the need for and use of costly, often clinically unnecessary, medical services and arbitrary managed-care interventions while improving the overall quality of life of patients. The Company believes that its system can be used to provide automated or semi-automated demand management services. The Company is currently providing demand management services in connection with programs that are intended to reach approximately 40,000 patients. Outcomes Analysis The Company intends to utilize information gathered from patients enrolled in its programs to serve two purposes. First, information regarding treatment results, success of the compliance program and patient reaction to differing treatments or compliance protocols may be used by the Company to further improve each disease-specific compliance program. Second, this information may be used by payors, pharmaceutical companies and health care providers to assist in the development of improved treatment modalities. The Company has developed analytical methodologies using database management and information technologies. The Company intends to use these data analysis technologies to predict the best treatment methodologies for patients. Clinical Studies Many pharmaceutical companies and contract research organizations are seeking more economical, efficient and reliable methods for compiling and analyzing clinical data in conducting clinical trials. Furthermore, many drug development protocols have begun to emphasize subjective criteria and outcomes information. The Company believes that its system will allow it to develop programs tailored to the measurement of outcomes data relating to the conduct of later stage clinical trials. The Company believes that its system can also assist pharmaceutical companies in studying and documenting the efficacy of approved products in order to provide ongoing information to FDA or for marketing purposes. Patient Surveys Organizations in many different areas of the health care industry survey users regarding their products and services for a variety of reasons including regulatory, marketing and research purposes. The Company's information systems, with their ability to proactively contact patients in a cost-efficient manner, may be used for this type of application. The Company is developing a series of 10 automated surveys ranging from general health to disease specific instruments. The product line includes surveys for SF-12; child health questionnaire; patient satisfaction; asthma; diabetes; back pain; depression; prostatis; maternity; and the Pra Plus for elderly populations. Case Management Patients who are prescribed complex or high cost treatment regimens may require a higher level of monitoring, interaction, care planning and reassessment than patients with less complicated treatment regimens. The Company believes that its system is capable of providing these enhanced services to such patients to eliminate or minimize the unnecessary costs and medical attention that result from a patient's lack of compliance with a prescribed treatment regimen. Sales and Marketing Through 1997, the Company's efforts focused primarily on the development of disease management programs. During 1997, the Company began aggressively marketing the other services that its technology platform can provide including demand management, patient surveys and outcomes analysis. The Company markets its integrated disease state management system to organizations within the health care industry that are involved in the treatment of disease or payment of medical services for patients who require complex or long-term medical therapies. These industry organizations include five distinct groups: pharmaceutical companies, medical service companies, PBMs, health care payors and employer groups. The Company employs a sales and marketing staff of eight persons to market the Company's systems. In addition, the senior members of the Company's management are actively engaged in marketing the Company's programs. The Company has expanded its marketing efforts by conducting patient surveys, clinical studies and implementing other measures designed to document the clinical and cost benefits it believes will result from the application of its integrated information capture and delivery system. In collaboration with the members of its expert panels who are retained to develop program protocols and other research and clinical technicians, the Company intends to promote the benefits of its system through publication in clinical journals and presentations at scientific conferences of the results of these studies. The Company is conducting such studies designed to produce significant short-term data with respect to its asthma and cardiac programs. Research and Development Research and development expenses consist primarily of salaries and related benefits and administrative costs allocated to the Company's research and development personnel for development of certain components of its integrated information capture and delivery system, as well as development of the Company's standardized disease state management programs. Research and development expenses were $489,115 for the year ended December 31, 1997, and $310,552 for the year ended December 31, 1996 and $89,909 for the period from February 1995 (inception) to December 31, 1995. The increase in these costs from 1995 to 1997 reflects initiation of development of the Company's standardized disease state management programs for patients suffering from asthma and diabetes. The development and maintenance of the telecommunications and computer publishing systems through which the Company operates its integrated information capture and delivery system is a major component of its business. The communications and information technology industries are subject to rapid and significant technological change, and the ability of the Company to operate and compete is dependent in significant part on its ability to update and enhance its system continuously. In order to do so, the Company must be able to utilize effectively its research and development capabilities and implement new technology in order to enhance its systems. At the same time, the Company must not jeopardize its ability to contact patients and to process and publish patient information or adapt to customer preferences or needs. The Company will maintain a significant investment in its technology, and therefore is subject to the risk of technological obsolescence. Competition The market for health care information products and services is intensely competitive. Competitors vary in size and in scope and breadth of products and services offered, and the Company competes with various companies in each of its disease target markets. Many of the Company's competitors have significantly greater financial, technical, product development and marketing resources than the Company. Furthermore, other major information, pharmaceutical and health care companies not presently offering disease state management or other health care information services may enter the markets in which the Company intends to compete. In addition, with sufficient financial and other resources, many of these competitors may provide services similar to those of the Company without substantial barriers. The Company does not possess any patents with respect to its integrated information capture and delivery system, and although it has filed a patent application with respect to certain aspects of its integrated information capture and delivery system and its integrated disease state management system, there can be no assurance that this application will result in the issuance of a patent, or if issued, that a patent would provide the Company with any competitive advantage. The Company's potential competitors include specialty health care companies, health care information system and software vendors, health care management organizations, pharmaceutical companies and other service companies within the health care industry. Many of these competitors have substantial installed customer bases in the health care industry and the ability to fund significant product development and acquisition efforts. The Company will also compete against other companies that provide statistical and data management services, including clinical trial services to pharmaceutical companies. The Company is aware of several large pharmaceutical and medical service companies that have publicly stated that they intend to be involved in providing comprehensive disease state management services. The Company believes that the principal competitive factors in its market are the ability to link patients, health care providers and payors, and provide the relevant health care information at an acceptable cost. In addition, the Company believes that the ability to anticipate changes in the health care industry and identify current needs are important competitive factors. Quality Control The Company has developed quality control measures designed to insure that information obtained from patients is accurately transcribed, that reports covering each patient contact are delivered to health care providers and patients and that the Company's personnel and technologies are interacting appropriately with patients and health care providers. Quality control systems include random monitoring of telephone calls, patient surveys to confirm patient participation and effectiveness of the particular program, and supervisory reviews of telephone agents. Government Regulation The health care industry, including the current and proposed business of the Company, is subject to extensive regulation by both the Federal and state governments. A number of states have extensive licensing and other regulatory requirements applicable to companies that provide health care services. Additionally, services provided to health benefit plans in certain cases are subject to the provisions of the Employee Retirement Income Security Act ("ERISA") and may be affected by other state and Federal statutes. Generally, state laws prohibit the practice of medicine and nursing without a license. Many states interpret the practice of nursing to include health teaching, health counseling, the provision of care supportive to or restorative of life and well being and the execution of medical regimens prescribed by a physician. Accordingly, to the extent that the Company assists providers in improving patient compliance by publishing educational materials or providing behavior modification training to patients, such activities could be deemed by a state to be the practice of medicine or nursing. Although the Company has not conducted a survey of the applicable law in all 50 states, it believes that it is not engaged in the practice of medicine or nursing. There can be no assurance, however, that the Company's operations will not be challenged as constituting the unlicensed practice of medicine or nursing. If such a challenge were made successfully in any state, the Company could be subject to civil and criminal penalties under such state's law and could be required to restructure its contractual arrangements in that state. Such results or the inability to successfully restructure its contractual arrangements could have a material adverse effect on the Company. The confidentiality of patient information is subject to regulation by state law. A variety of statutes and regulations exist safeguarding privacy and regulating the disclosure and use of medical information. State constitutions may provide privacy rights and states may provide private causes of action for violations of an individual's "expectation of privacy." Tort liability may result from unauthorized access and breaches of patient confidence. The Company intends to comply with state law and regulations governing medical information privacy. In addition, on August 21, 1996 Congress passed the Health Insurance Portability and Accountability Act of 1996, P.L. 104-191. This legislation requires the Secretary of Health and Human Services to adopt national standards for electronic health transactions and the data elements used in such transactions. The Secretary is required to adopt safeguards to ensure the integrity and confidentiality of such health information. Violation of the standards is punishable by fines and, in the case of wrongful disclosure of individually identifiable health information, imprisonment. The Secretary is required to issue the standards not later than February 21, 1998. The Company cannot predict what requirements will ultimately be adopted by the Secretary, however, such requirements could have an adverse effect on the Company's business. The Company and its customers may be subject to Federal and state laws and regulations which govern financial and other arrangements between health care providers. These laws prohibit certain fee splitting arrangements between health care providers, as well as direct and indirect payments, referrals or other financial arrangements that are designed to induce or encourage the referral of patients to, or the recommendation of, a particular provider for medical products and services. Possible sanctions for violation of these restrictions include civil and criminal penalties. Further, criminal violations may result in mandatory exclusions of up to five years and additional permissive exclusions from participation in Medicare and Medicaid programs. Regulation in the health care field is constantly evolving. The Company is unable to predict what government regulations, if any, affecting its business may be promulgated in the future. The Company's business could be adversely affected by the failure to obtain required licenses and governmental approvals, comply with applicable regulations or comply with existing or future laws, rules or regulations or their interpretations. Intellectual Property The Company considers its methodologies, processes and know-how to be proprietary. The Company seeks to protect its proprietary information through confidentiality agreements with its employees. The Company's policy is to have employees enter into confidentiality agreements containing provisions prohibiting the disclosure of confidential information to anyone outside the Company, requiring employees to acknowledge, and, if requested, assist in confirming the Company's ownership of any new ideas, developments, discoveries or inventions conceived during employment, and requiring assignment to the Company of proprietary rights to such matters that are related to the Company's business. The Company has filed a patent application with respect to certain aspects of its integrated information capture and delivery and integrated disease state management systems. No assurance can be given that a patent will issue or that if issued such patent will provide the Company with a competitive advantage. Employees As of February 28, 1998, the Company had 67 full and part-time employees. Item 2. Description of Properties. The Company's executive and corporate offices are located in Rochester, New York in approximately 13,000 square feet of leased office space under an operating lease that expires on November 30, 1999. Item 3. Legal Proceedings. The Company is not a party to any material legal proceedings. Item 4. Submission of Matters To A Vote Of Security Holders. No matters were submitted to a vote of security holders during the fourth quarter ended December 31, 1997. PART II Item 5. Market Price of and Dividends on the Registrant's Common Equity and Related Stockholder Matters. (a) Market Information The Company's common stock is traded on the NASDAQ National Market System under the symbol "PATI". The following table sets forth, for the periods indicated, the range of the high and low sales prices for the Company's Common Stock as reported on the Nasdaq National Market beginning in the fourth quarter of 1996. High Low 1996 Fourth Quarter $9.25 $8.00 1997 First Quarter $9.25 $6.38 Second Quarter $6.25 $4.50 Third Quarter $5.00 $2.88 Fourth Quarter $4.38 $2.63 (b) Holders The approximate number of holders of the Company's common stock as of February 28, 1998 is 99. However, the Company believes that there are in excess of 400 beneficial holders of Common Stock of the Company. (c) Dividends The Company has never paid cash dividends on its capital stock and does not anticipate paying any cash dividends in the foreseeable future. The Company currently intends to retain all future earnings, if any, to fund the development and growth of its business. Any future determination to pay cash dividends will be at the discretion of the Board of Directors. Item 6. Selected Financial Data.
Period from February 22, 1995 Year Ended Year Ended (Inception) to December 31, December 31, December 31, 1997 1996 1995 ---- ---- ---- Statement of Operations Data: Revenues $ 2,062,373 $ 845,412 $ 113,000 ---------- --------- --------- Costs and Expenses: Cost of Sales 1,629,128 748,322 111,870 Sales and Marketing 1,609,837 913,547 375,384 General and Administrative 2,432,760 1,760,760 678,498 Research and Development 489,115 310,552 89,909 ------- ------- ------ Total Costs and Expenses 6,160,840 3,733,181 1,255,661 --------- --------- -------- Operating Loss (4,098,467) (2,887,769) (1,142,661) Interest Income 835,116 81,333 26,009 ------- ------ ------ Net Loss $(3,263,351) $(2,806,436) $(1,116,652) =========== =========== =========== Net Loss Per Share - Basic and Diluted $ (.41) $ (.44) $ (0.18) =========== =========== =========== Weighted Average Common and Potential Common Shares 7,980,094 6,347,716 5,954,299 ========= ========= ========= December 31, 1997 1996 1995 ---- ---- ---- Balance Sheet Data: Cash and Cash Equivalents $ 779,317 $15,666,609 $ 1,182,080 Working Capital 13,242,387 14,591,700 611,655 Total Assets 15,036,473 17,085,387 1,763,629 Total Liabilities 587,728 1,631,650 598,464 Total Stockholders' Equity 14,448,745 15,453,737 1,165,165
Item 7. Management's Discussion and Analysis of Financial Condition and Results of Operations. Management's discussion and analysis provides a review of the Company's operating results for the years ended December 31, 1997 and 1996 and the period from inception on February 22, 1995 to December 31, 1995, and its financial condition at December 31, 1997. The focus of this review is on the underlying business reasons for significant changes and trends affecting the revenues, net earnings, and financial condition of the Company. This review should be read in conjunction with the accompanying financial statements. In an effort to give investors a well-rounded view of the Company's current condition and future opportunities, this Annual Report on Form 10-K includes forecasts by the Company's management about future performance and results. Because they are forward-looking, these forecasts involve uncertainties. They include risks of market acceptance of or preference for the Company's systems and services, competitive forces, the impact of, and changes in, government regulations, general economic factors in the healthcare industry, and other factors discussed in the Company's filings with the Securities and Exchange Commission. Overview The Company was formed on February 22, 1995 and has a limited operating history from which to evaluate its performance. Although the Company has completed the development of its integrated information capture and delivery system and is developing several disease state management programs for specific diseases, further development activities may be necessary to implement these programs. In October 1996 the Company began enrolling patients in its first disease state management program, and even though over a year has passed, the Company currently has patients enrolled in four of its disease-specific programs. The enrollment of patients in the Company's programs has been limited by several factors, including the limited ability of clients to provide the Company with accurate information with respect to the specific patient populations, including coding errors that necessitated significant labor-intensive data processing prior to program implementation. In addition, the Company has encountered resistance from patients and other sources of information to the Company's systems. In response to these market dynamics, the Company has taken several tactical and strategic steps: formal designation of internal personnel at customer sites to assist clients with implementation; closer integration of Company systems personnel with clients to facilitate accurate data transfers; and most importantly, promotion of a broader product line to enable clients to enter the Company's disease management programs through a variety of channels. The Company now sells two additional services, demand management services and automated surveys (general health and disease-specific), both of which can provide mechanisms for enrollment to the Company's disease management programs. Through February 1998, an aggregate of approximately 38,000 persons have enrolled and participated in Company programs. The Company has entered into services agreements to develop, implement and operate programs for: (i) patients who have recently experienced certain cardiovascular events; (ii) patients who have been diagnosed with primary congestive heart failure; (iii) patients suffering from anorexia or cachexia secondary to diagnosis of cancer or AIDS; (iv) patients suffering from chronic pain, and (v) patients who are at increased risk of suffering from epilepsy. In addition, the Company has entered into services agreements to operate its disease management programs for patients suffering from asthma or diabetes. These contracts provide for, and the Company anticipates future contracts will provide for, fees paid by its customers based upon the number of patients participating in each of its programs, as well as initial program development fees from customers for the development of a disease-specific program. To the extent that the Company has had limited enrollment of patients in its programs, the Company's operations revenue has been, and may continue to be limited. Moreover, as the Company has completed the development of its primary disease management programs, it anticipates that development revenue will also decline over the next twelve months unless and until the Company enters into new development agreements. The Company's program development contracts typically require payment from the customer at the time that the contract is executed, with additional payments made as certain development milestones are met. Development contract revenue is recognized on a percentage of completion basis, in accordance with the ratio of total development cost incurred to the estimated total development costs for the entire project. Losses, if any, related to program development will be recognized in full as identified. The Company's contracts call for a fixed program operational fee to be paid by the customer for each patient enrolled for a series of program services as defined in the contract. The timing of customer payments for the delivery of program services varies by contract. Revenues from program operations are recognized ratably as the program services are delivered. The amount of the per patient fee varies from program to program depending upon the number of patient contacts required, the complexity of the interventions and the detail of the reports generated. The Company has not capitalized any costs related to the development of software for use in its disease state management programs since all of such software has been developed for internal use. The sales cycle for the Company's programs is expected to extend for periods of six to nine months from initial contact to contract execution. During these periods, the Company may expend substantial time, effort and funds to prepare a contract proposal and negotiate the contract. The Company may be unable to consummate a commercial relationship after the expenditure of such time, effort and financial resources. The Company began to provide other services to customers in the healthcare industry during 1997 which included new applications of its information capture and delivery system. These consisted of patient surveys, health risk assessments, nursing support lines and marketing support functions. It is anticipated that the revenues generated from services other than those provided in conjunction with disease state management programs will represent an increasing percentage of total revenues as the Company continues to expand the systems and services that it makes available to its customers. Results of Operations Year Ended December 31, 1997 Compared to Year Ended December 31, 1996 Revenues Revenues are comprised of revenues from development fees, licensing fees and operational fees. Revenues increased 144% from $845,412 for the year ended December 31, 1996 to $2,062,373 for the year ended December 31, 1997. A summary of these revenues by category is as follows: Year Ended Year Ended December 31, December 31, 1997 1996 ---- ---- Revenues -------- Development Fees $ 826,532 $798,138 Licensing Fees 500,000 35,556 Operational Fees 735,841 11,718 ------- ------ Total Revenues $2,062,373 $845,412 ========== ======== Revenues from development fees increased 3.6% from $798,138 for the year ended December 31, 1996 to $826,532 for the year ended December 31, 1997. The Company received $826,532 in development revenues for the year ended December 31, 1997, primarily related to fees from Bristol-Myers for the development of six disease state management contracts. The Company also received development revenues from a small number of other customers related to other disease-specific programs. The Company has completed substantially all services under these agreements and is currently receiving revenues in connection with only the development of three programs. The Company anticipates that revenue from development fees will decline as the Company develops more programs using its own resources. The Company's development contracts generally require that payments be made by the customer at the time of contract execution and at the achievement of certain milestones in the development process. These payments are normally received in advance of the Company's recognition of the associated revenue. The timing of customer payments for program operation services varies by contract, but typically occurs prior to the associated services being provided. The Company recognizes deferred revenue for amounts billed for these services in advance of the rendering of the services. The advance payments have been a source of liquidity for the Company. The Company anticipates that its billing practices are likely to continue in this manner in the foreseeable future. Revenues from licensing fees increased 1306% from $35,556 for the year ended December 31, 1996 to $500,000 for the year ended December 31, 1997. Licensing revenue represents amounts that the Company charges its customers for the right to enroll patients in or the right to market to other entities certain of its programs, primarily the Company's standardized asthma and diabetes programs, and the right to have access to data collected from patients enrolled in such programs. The Company did not initiate any licensing activity until the second quarter of 1996, therefore licensing revenues for the year ended December 31, 1997 were significantly higher that those generated during the year ended December 31, 1996. In 1997, the Company received licensing revenues of $150,000 from the PulseGroup, Inc. for a licensing contract related to the Company's asthma and diabetes programs. Revenues from operations increased 6180% from $11,718 for the year ended December 31, 1996 to $735,841 for the year ended December 31, 1997. Operations revenues are generated as the Company provides services to its customers for their disease-specific programs. Operations revenues increased significantly in 1997, as the Company began enrolling patients and implementing its disease state management programs during 1997. Operations revenue consisted primarily of $440,000 in fees received from Abbott Laboratories in connection with a teleconference program completed during the year ended December 31, 1997. The Company is currently engaged in discussions with Abbott Laboratories with respect to providing additional services to Abbott Laboratories in the future. The Company began to provide other services to customers in the healthcare industry during 1997 which involve new applications of its information capture and delivery system. These services include patient surveys, health risk assessments, nursing support lines and marketing support functions. As the Company expands its operations, it intends to continue to emphasize operations revenues to the exclusion of development revenues. Costs and Expenses Cost of sales include salaries and related benefits, services provided by third parties, and other expenses associated with the development of the Company's customized disease state management programs, as well as the operation of each of its disease state management programs. In addition, cost of sales for 1997 and 1996 includes accrued losses on program development in accordance with the Company's policy of recognizing such losses, if any, in full as identified. The accrued loss for 1997 and 1996 is a result of a particular contract for which the amount of the program development fee is based upon the success of the program, and the fact that the guaranteed development revenue for this program is less than the estimated cost of its development. To the extent that the Company enters into any contracts of this type in the future, and that those contracts provide for guaranteed development revenue which is less than the estimated cost of program development, such losses will continue to be accrued. Cost of sales increased 118% from $748,322 for the year ended December 31, 1996 to $1,629,128 for the year ended December 31, 1997. The increase in these costs primarily reflects an increased level of program development and operational activities. Sales and marketing expenses increased 76% from $913,547 for the year ended December 31, 1996 to $1,609,837 for the year ended December 31, 1997. These costs consist primarily of salaries, related benefits and travel costs. These expenditures allowed the Company to undertake initial marketing efforts to pharmaceutical companies, payors and other health care services organizations. The increase in these costs reflects an increase in the size of the Company's sales and marketing staff. General and administrative expenses include the costs of corporate operations, finance and accounting, human resources and other general operating expenses of the Company. General and administrative expenses increased 38% from $1,760,760 for the year ended December 31, 1996 to $2,432,760 for the year ended December 31, 1997. These expenditures were incurred to develop the corporate infrastructure necessary to support anticipated program development and operations. The increase in these costs was caused by an increase in the Company's level of business activity, and the addition of required administrative personnel. The Company expects that general and administrative expenses will continue to increase in future periods. Research and development expenses consist primarily of salaries and related benefits and administrative costs allocated to the Company's research and development personnel for development of certain components of its integrated information capture and delivery system, as well as development of the Company's standardized disease state management programs. Research and development expenses increased 57% from $310,552 for the year ended December 31, 1996 to $489,115 for the year ended December 31, 1997. The increase in these costs reflects initiation of development of the Company's standardized disease state management programs for patients suffering from asthma and diabetes. The Company generates net interest income primarily from cash balances and investments. Interest income increased to $835,116 for the year ended December 31, 1997 from $81,333 for the year ended December 31, 1996. The increase in interest income reflects the additional funds available to the Company for investment as a result of its initial public offering on December 19, 1996. The Company had a net loss of $3,263,351 for the year ended December 31, 1997 compared to $2,806,436 for the year ended December 31, 1996. This represents a loss of $.41 per share for 1997 and $.44 for 1996. Year Ended December 31, 1996 Compared to the Period from February 1995 (Inception) to December 31, 1995 Revenues The Company generated revenue of $845,412 for the year ended December 31, 1996, and $113,000 during the period from inception on February 22, 1995 to December 31, 1995. A summary of these revenues by category is as follows: Period from February 1995 Year Ended (Inception) to December 31, 1996 December 31, 1995 ----------------- ----------------- Revenues -------- Development Fees $798,138 $84,000 Licensing Fees 35,556 - Operational Fees 11,718 29,000 ------ ------ Total Revenues $845,412 $113,000 ======== ======== The increase in program development fees reflects the increase in the level of development activities for the Company's customized programs. The increase in program licensing fees reflects the initiation of licensing of the Company's standardized programs. Revenues from program operations are not significant because patient enrollments in the Company's disease state management programs were not initiated until October 1996. Costs and Expenses Cost of sales include salaries and related benefits, services provided by third parties, and other expenses associated with the development of the Company's customized disease state management programs, as well as the operation of each of its disease state management programs. In addition, cost of sales for 1996 includes accrued losses on program development in accordance with the Company's policy of recognizing such losses, if any, in full as identified. The accrued loss for 1996 is a result of a particular contract for which the amount of the program development fee is based upon the success of the program, and the fact that the guaranteed development revenue for this program is less than the estimated cost of its development. To the extent that the Company enters into any contracts of this type in the future, and that those contracts provide for guaranteed development revenue which is less than the estimated cost of program development, such losses will continue to be accrued. Cost of sales was $748,322 for the year ended December 31, 1996, and $111,870 for the period from inception on February 22, 1995 to December 31, 1995. The increase in these costs primarily reflects an increased level of program development activities. Sales and marketing expenses for the year ended December 31, 1996 were $913,547, and $375,384 for the period from inception on February 22, 1995 to December 31, 1995. These costs consist primarily of salaries, related benefits and travel costs. These expenditures allowed the Company to undertake initial marketing efforts to pharmaceutical companies, payors and other health care services organizations. The increase in these costs reflects an increase in the size of the Company's sales and marketing staff. General and administrative expenses include the costs of corporate operations, finance and accounting, human resources and other general operating expenses of the Company. General and administrative expenses for the year ended December 31, 1996 were $1,760,760, and $678,498 for the period from inception on February 22, 1995 to December 31, 1995. These expenditures were incurred to develop the corporate infrastructure necessary to support anticipated program development and operations. The increase in these costs was caused by an increase in the Company's level of business activity, and the addition of required administrative personnel. Research and development expenses consist primarily of salaries and related benefits and administrative costs allocated to the Company's research and development personnel for development of certain components of its integrated information capture and delivery system, as well as development of the Company's standardized disease state management programs. Research and development expenses for the year ended December 31, 1996 were $310,552, and $89,909 for the period from inception on February 22, 1995 to December 31, 1995. The increase in these costs reflects initiation of development of the Company's standardized disease state management programs for patients suffering from asthma and diabetes. During 1996 each of the Company's categories of costs and expenses decreased as a percentage of revenues from the prior period, despite the fact that they increased in absolute dollars, due to the significant increase in the Company's revenues during 1996. Interest income was $81,333 for the year ended December 31, 1996, and $26,009 for the period from inception on February 22, 1995 to December 31, 1995. The increase in interest income reflects the additional funds available to the Company for investment as a result of its initial public offering on December 19, 1996. The Company had a net loss of $2,806,436 for the year ended December 31, 1996, and a loss of $1,116,652 for the period from inception on February 22, 1995 to December 31, 1995. This represents a loss of $.44 per share for 1996, and a loss of $.18 per share for the period from inception on February 22, 1995 to December 31, 1995. Liquidity and Capital Resources At December 31, 1997 the Company had working capital of $13,242,387, as compared to $14,591,700 at December 31, 1996 and $611,655 at December 31, 1995. Since its inception the Company has primarily funded its operations, working capital needs and capital expenditures from the sale of equity securities. The Company's initial capitalization of $500,000 was completed in February 1995. The Company received $1,800,000 from the sale of equity securities in a private placement during the third quarter of 1995, and $3,000,000 from the sale of additional equity securities in a private placement during the second quarter of 1996. On December 19, 1996 the Company completed an initial public offering of its common stock which generated net proceeds to the Company of $14,082,048. On January 8, 1997, an additional 300,000 shares of common stock were sold pursuant to an underwriters over-allotment provision, which generated net proceeds to the Company of $2,232,000. Capital expenditures during 1997 were $394,161, as compared to expenditures of $494,577 during 1996 and $579,983 during the period from inception on February 22, 1995 to December 31, 1995. The expenditures during these periods represented the purchase of the significant technology platform components of the integrated information capture and delivery system as well as purchases required to support the Company's growing employee base. The Company has been substantially dependent upon the public and private sale of securities to fund its research and development activities and working capital requirements. In order to implement programs using the Company's integrated information capture and delivery system, the Company will be required to devote substantial additional assets to the development of technology, the construction of physical facilities and the acquisition of telephone and computer equipment. The Company will also be required to retain the services of employees in advance of obtaining contracts to provide services. Inflation Inflation did not have a significant impact on the Company's costs during 1997, 1996 or the period from inception on February 22, 1995 to December 31, 1995. The Company continues to monitor the impact of inflation in order to minimize its effects through pricing strategies, productivity improvements and cost reductions. Recent Accounting Pronouncements In March 1997, the Financial Accounting Standards Board (FASB) issued Statement of Financial Accounting Standards (SFAS) No. 128, "Earnings Per Share". The new standard requires dual presentation of basic and diluted earnings per share (EPS) on the face of the statement of operations and requires a reconciliation of the numerators and denominators of basic and diluted EPS calculations. The statement is effective for periods ending after December 15, 1997. In June 1997, the Financial Accounting Standards Board (FASB) issued Statement of Financial Accounting Standards No. 130, "Reporting Comprehensive Income," which is required to be adopted for fiscal years beginning after December 15, 1997. This statement establishes standards for reporting and display of comprehensive income and its components in a full set of general-purpose financial statements. This statement requires that all items that are required to be recognized under accounting standards as components of comprehensive income to be reported in a financial statement that is displayed with the same prominence as other financial statements. Comprehensive income is defined as the change in equity of a business enterprise during a period from transactions and other events and circumstances from non-owner sources. Items considered comprehensive income include foreign currency items, minimum pension liability adjustments and unrealized gains and losses on certain investments in debt and equity securities. In the opinion of management, SFAS 130 will not have a material effect on the Company's financial statements. In June 1997 the Financial Accounting Standards Board issued Statement of Financial Accounting Standards No. 131, "Disclosures about Segments of an Enterprise and Related Information," effective for fiscal years beginning after December 15, 1997. The statement requires that a public company report financial and descriptive information about its reportable operating segments using the management approach. In the opinion of management, SFAS 131 will not have a material effect on the Company's financial statements. In October 1997, the Accounting Standards Executive Committee issued Statement of Position (SOP) 97-2, "Software Revenue Recognition," which provides guidance on applying generally accepted accounting principles in recognizing revenue on software transactions and is effective for transactions entered into in fiscal years beginning after December 15, 1997. The Company does not believe that the implementation of SOP 97-2 will have a material effect on expected revenues or earnings. Year 2000 The Company has conducted a review of its computer systems to identify those areas that could be affected by the "Year 2000" issue and is developing an implementation plan to resolve the issue. The Company currently believes, with planned modifications to existing software and converting to new software, the Year 2000 problem will not pose significant operational problems and is not anticipated to be material to its financial position or results of operations in any given year. The Company has received confirmation from vendors of certain purchased software that current releases or upgrades, if installed, will eliminate any issues. Forward Looking Statements When used in this and in future filings by the Company with the Securities and Exchange Commission, in the Company's press releases and in oral statements made with the approval of an authorized executive officer of the Company, the words or phrases "will likely result," "expects," "plans," "will continue," "is anticipated," "estimated," "project," or "outlook" or similar expressions (including confirmations by an authorized executive officer of the Company of any such expressions made by a third party with respect to the Company) are intended to identify "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995. The Company wishes to caution readers not to place undue reliance on any such forward-looking statements, each of which speak only as of the date made. Such statements are subject to certain risks and uncertainties that could cause actual results to differ materially from historical earnings and those presently anticipated or projected. The Company has no obligation to publicly release the result of any revisions which may be made to any forward-looking statements to reflect anticipated or unanticipated events or circumstances occurring after the date of such statements. 2 Item 8. Financial Statements And Supplemental Data Index to Financial Statements Page Independent Auditors' Report 24 Balance Sheets 25 Statements of Operations 26 Statements of Stockholders' Equity 27 Statements of Cash Flows 28 Notes to Financial Statements 29-34 INDEPENDENT AUDITORS' REPORT To the Board of Directors and Stockholders of Patient Infosystems, Inc.: We have audited the accompanying balance sheets of Patient Infosystems, Inc. as of December 31, 1997 and 1996 and the related statements of operations, stockholders' equity, and cash flows for the years ended December 31, 1997 and 1996 and for the period from February 22, 1995 (Inception) to December 31, 1995. 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. Deloitte & Touche LLP Rochester, New York January 30, 1998 PATIENT INFOSYSTEMS, INC. BALANCE SHEETS DECEMBER 31, 1997 AND 1996 - --------------------------------------------------------------------------------
ASSETS 1997 1996 CURRENT ASSETS: Cash and cash equivalents ........................ $ 779,317 $15,666,609 Available-for-sale securities .................... 12,232,335 -- Accounts receivable .............................. 412,956 386,215 Prepaid expenses and other current assets ........ 405,507 170,526 ---------- ----------- Total current assets ....................... 13,830,115 16,223,350 PROPERTY AND EQUIPMENT, net ........................ 958,965 862,037 OTHER ASSETS ....................................... 247,393 -- ----------- ----------- TOTAL ASSETS ....................................... $15,036,473 $17,085,387 =========== =========== LIABILITIES AND STOCKHOLDERS' EQUITY CURRENT LIABILITIES: Accounts payable ................................. $ 89,674 $ 196,674 Accrued salaries and wages ....................... 320,272 127,029 Accrued initial public offering costs ............ -- 446,568 Accrued expenses ................................. 79,236 211,457 Deferred revenue ................................. 67,549 582,783 Accrued loss on development contracts ............ 30,997 67,139 ------------ ------------ Total current liabilities .................. 587,728 1,631,650 ------------ ------------ COMMITMENTS (Note 7) STOCKHOLDERS' EQUITY: Common stock - $.01 par value: shares - authorized: 20,000,000; issued and outstanding: 1997 - 8,011,522 1996 - 7,653,202 ............................... 80,115 76,532 Additional paid-in capital ....................... 21,550,009 19,300,293 Unrealized gain on available-for-sale securities . 5,060 -- Accumulated deficit during the development stage . (7,186,439) (3,923,088) ----------- ----------- Total stockholders' equity ................. 14,448,745 15,453,737 ----------- ------------ TOTAL LIABILITIES AND STOCKHOLDERS' EQUITY ........ $ 15,036,473 $ 17,085,387 ============ ============
See notes to financial statements. PATIENT INFOSYSTEMS, INC. STATEMENTS OF OPERATIONS YEARS ENDED DECEMBER 31, 1997 AND 1996 AND PERIOD FROM FEBRUARY 22, 1995 (INCEPTION) TO DECEMBER 31, 1995 - --------------------------------------------------------------------------------
1997 1996 1995 REVENUES ....................... $ 2,062,373 $ 845,412 $ 113,000 ----------- ----------- ----------- COSTS AND EXPENSES: Cost of sales ................ 1,629,128 748,322 111,870 Sales and marketing .......... 1,609,837 913,547 375,384 General and administrative ... 2,432,760 1,760,760 678,498 Research and development ..... 489,115 310,552 89,909 ----------- --------- --------- Total costs and expenses 6,160,840 3,733,181 1,255,661 ----------- ----------- --------- OPERATING LOSS ................. (4,098,467) (2,887,769) (1,142,661) INTEREST INCOME ................ 835,116 81,333 26,009 ---------- ---------- ---------- NET LOSS ....................... $(3,263,351) $(2,806,436) $(1,116,652) =========== =========== =========== NET LOSS PER SHARE - BASIC AND DILUTED ................. $ (.41) $ (.44) $ (.18) =========== =========== =========== WEIGHTED AVERAGE COMMON AND POTENTIAL COMMON SHARES . 7,980,094 6,347,716 5,954,299 =========== =========== ===========
See notes to financial statements. PATIENT INFOSYSTEMS, INC. STATEMENTS OF STOCKHOLDERS' EQUITY YEARS ENDED DECEMBER 31, 1997 AND 1996 AND PERIOD FROM FEBRUARY 22, 1995 (INCEPTION) TO DECEMBER 31, 1995 - --------------------------------------------------------------------------------
Unrealized Additional Gains/Losses on Total Preferred Stock Common Stock Paid-in Available-for-sale Accumulated Stockholders' Shares Amount Shares Amount Capital Securities Deficit Equity Sale of common stock, substantially all of which was issued on February 22, 1995 at $0.14 per share - $ - 3,602,880 $36,029 $ 464,371 $ - $ - $ 500,400 Sale of Series A convertible preferred stock at $1.00 per share in August and September 1995 (net of issuance costs of $18,583) 1,800,000 18,000 - - 1,763,417 - - 1,781,417 Net loss for the period from Inception to December 31, 1995 - - - - - - (1,116,652) (1,116,652) --------- ------ --------- ------- ----------- ------ ---------- ---------- Balances, December 31, 1995 1,800,000 18,000 3,602,880 36,029 2,227,788 - (1,116,652) 1,165,165 Sale of Series B convertible preferred stock at $5.00 per share in May and June 1996 (net of issuance costs of $3,250) 600,000 6,000 - - 2,990,750 - - 2,996,750 Compensation expense related to issuance of stock warrants - - - - 13,208 - - 13,208 Exercise of stock warrants - - 4,322 43 2,959 - - 3,002 Sale of common stock at $8.00 per share in December 1996 (net of issuance costs of $1,917,952) - - 2,000,000 20,000 14,062,048 - - 14,082,048 Conversion of Series A and B convertible preferred stock to common stock (2,400,000) (24,000) 2,046,000 20,460 3,540 - - - Net loss for the year end December 31, 1996 - - - - - - (2,806,436) (2,806,436) --------- ------ --------- ------ ---------- ------ --------- --------- Balances, December 31, 1996 - - 7,653,202 76,532 19,300,293 - (3,923,088) 15,453,737 Sale of common stock at $8.00 per share in January 1997 (net of issuance costs of $168,000) - - 300,000 3,000 2,229,000 - - 2,232,000 Compensation expense related to issuance of stock warrants - - - - 8,283 - - 8,283 Exercise of stock warrants - - 58,320 583 12,433 - - 13,016 Unrealized gain on investments available for sale - - - - - 5,060 - 5,060 Net loss for the year end December 31, 1997 - - - - - - (3,263,351) 3,263,351) --------- ------ --------- ------- ----------- ------ ---------- ---------- Balances, December 31, 1997 - $ - 8,011,522 $80,115 $21,550,009 $5,060 $(7,186,439) $14,448,745 ========= ====== ========= ======= =========== ====== ============ ===========
See notes to financial statements. PATIENT INFOSYSTEMS, INC. STATEMENTS OF CASH FLOWS YEARS ENDED DECEMBER 31, 1997 AND 1996 AND PERIOD FROM FEBRUARY 22, 1995 (INCEPTION) TO DECEMBER 31, 1995 - --------------------------------------------------------------------------------
1997 1996 1995 OPERATING ACTIVITIES: Net loss ....................................................... $(3,263,351) $(2,806,436) $(1,116,652) Adjustments to reconcile net loss to net cash used in operating activities: Depreciation and amortization .............................. 293,763 186,050 26,473 Loss on sale of property ................................... 2,171 -- -- Amortization of premiums and discounts on available-for-sale marketable securities ................................. (209,832) -- -- Compensation expense related to issuance of stock warrants ........................................... 8,283 13,208 -- Increase in accounts receivable ............................ (26,741) (382,160) (4,055) Increase in prepaid expenses and other current assets ...... (234,980) (146,542) (23,984) (Decrease) increase in accounts payable .................... (107,000) (166,095) 362,769 Increase in accrued salaries and wages ..................... 193,243 78,770 48,259 (Decrease) increase in accrued expenses .................... (132,221) 192,076 19,381 (Decrease) increase in deferred revenue .................... (515,234) 414,728 168,055 (Decrease) increase in accrued loss on development contracts (36,142) 67,139 -- --------- --------- --------- Net cash used in operating activities ................ (4,028,041) (2,549,262) (519,754) --------- --------- --------- INVESTING ACTIVITY: Property and equipment additions ............................... (394,161) (494,577) (579,983) Proceeds from sale of property ................................. 1,299 -- -- Purchases of available-for-sale marketable securities .......... (18,121,444) -- -- Maturities of available for-sale marketable securities ......... 6,104,000 -- -- Increase in other assets ....................................... (247,393) -- -- --------- --------- --------- Net cash used in investing activities ................. (12,657,699) (494,577) (579,983) ---------- --------- --------- FINANCING ACTIVITIES: Proceeds from issuance of common and preferred stock, net ................................................... 2,245,016 17,081,800 2,281,817 (Decrease) increase in accrued initial public offering costs ... (446,568) 446,568 -- --------- ---------- ---------- Net cash provided by financing activities ............ 1,798,448 17,528,368 2,281,817 --------- ---------- ---------- INCREASE (DECREASES) IN CASH AND CASH EQUIVALENTS ............... (14,887,292) 14,484,529 1,182,080 CASH AND CASH EQUIVALENTS AT BEGINNING OF PERIOD ............................................ 15,666,609 1,182,080 -- ---------- ---------- --------- CASH AND CASH EQUIVALENTS AT END OF PERIOD .................................................. $ 779,317 $15,666,609 $ 1,182,080 =========== =========== =========== Supplemental disclosures of cash flow information Cash paid and received for income taxes, net .................. $ (9,509) $ 1,716 $ -- =========== =========== ===========
See notes to financial statements ................................ PATIENT INFOSYSTEMS, INC. NOTES TO FINANCIAL STATEMENTS YEARS ENDED DECEMBER 31, 1997, 1996 AND PERIOD FROM FEBRUARY 22, 1995 (INCEPTION) TO DECEMBER 31, 1995 - -------------------------------------------------------------------------------- 1. BUSINESS AND SIGNIFICANT ACCOUNTING POLICIES Organization - Patient Infosystems, Inc. designs and develops health care information systems and services to manage, collect and analyze patient-related information to improve patient compliance with prescribed treatment protocols. Through its various patient compliance programs for disease state management, the Company provides important benefits for the patient, the health care provider and the payor. The Company was incorporated in Delaware on February 22, 1995 under the name DSMI Corp., changed its name to Disease State Management, Inc. on October 13, 1995, and on June 28, 1996 changed its name to Patient Infosystems, Inc. Prior to January 1, 1997, the Company was a development stage enterprise. Use of Estimates in the Preparation of Financial Statements - 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 and the reported amounts of revenues and expenses during the reporting period. Actual amounts could differ from those estimates. Fair Value of Financial Instruments - The Company's financial instruments consist of cash and equivalents and available-for-sale securities. The carrying values of cash and equivalents and available-for-sale marketable securities approximate fair value. Revenue Recognition and Deferred Revenue - The Company's principal source of revenue to date has been from contracts with a pharmaceutical company for the development and operation of disease management programs for chronic diseases, disease management programs and other health care information system applications. Deferred revenue represents amounts billed in advance under these contracts. Development Contracts - The Company's program development contracts typically require payment from the customer at the time that the contract is executed, with additional payments made as certain development milestones are met. Development contract revenue is recognized on a percentage of completion basis, in accordance with the ratio of total development cost incurred to the estimated total development costs for the entire project. Losses, if any, are recognized in full as identified. Program Operations - The Company's program operation contracts call for a per enrolled patient fee to be paid by the customer for a series of program services as defined in the contract. The timing of customer payments varies by contract, but typically occurs in advance of the associated services being provided. Revenues from program operations are recognized ratably as the program services are delivered. Cash and Cash Equivalents - Cash and cash equivalents include all highly liquid debt instruments with original maturities of three months or less. Concentrations of Credit Risk - Financial instruments which potentially subject the Company to concentration of credit risk consist principally of cash and cash equivalents and accounts receivable. The Company places its cash and cash equivalents with high credit quality institutions. The Company's current contracts are concentrated in a small number of customers, consequently, the loss of any one of its customers could have a material adverse effect on the Company and its operations. During the years ended December 31, 1997 and 1996, approximately $925,800 (45%) and $834,000 (99%), respectively, of the Company's revenues arose from contracts with one customer. At December 31, 1997 and 1996, accounts receivable included balances of $231,484 and $265,940, respectively, from contracts with that customer. Property and Equipment - Property and equipment are stated at cost. Depreciation is computed using the straight-line method over the estimated useful lives of the assets, which range from 3 to 10 years. The Company regularly assesses all of its long lived assets for impairment and recognizes a loss when the carrying value of an asset exceeds its fair value. The Company determined that no impairment loss need be recognized for applicable assets in 1997 or 1996. Research and Development - Research and development costs consist principally of compensation and benefits paid to Company employees. All research and development costs are expensed as incurred. Income Taxes - The Company uses the asset and liability method of accounting for income taxes in accordance with Statement of Financial Accounting Standards No. 109, "Accounting for Income Taxes". Under the asset and liability method, deferred income tax assets and liabilities are recognized for the future tax consequences attributable to differences between the financial statement carrying amounts of existing assets and liabilities and their respective tax bases and net operating loss and tax credit carryforwards. Net Loss Per Share - Net loss per share is based on the weighted average number of common shares outstanding subsequent to the Company's initial public offering in 1996. Pursuant to rules of the Securities and Exchange Commission Staff, all common and potential common shares issued by the Company at a price less than the initial public offering price during at least the 12 months preceding the offering date (using the treasury stock method until shares are issued) have been included in the calculation of common and potential common shares outstanding for all periods presented prior to the December 1996 initial public offering. Retirement Plan - The Company has a retirement plan which qualifies under Section 401(k) of the Internal Revenue Code This retirement plan allows eligible employees to contribute 1% to 15% of their income on a pretax basis to the plan. The Company's annual contribution to the plan is at the discretion of the Board of Directors. The Company made no contributions to this plan in 1997 or 1996. Stock Split - On November 22, 1996, the Company effected a .72-for-1 reverse stock split of all outstanding shares of common stock. Statement of Financial Accounting Standards No. 128 - In March 1997, the Financial Accounting Standards Board (FASB) issued Statement of Financial Accounting Standards (SFAS) No. 128, "Earnings Per Share". The new standard requires dual presentation of basic and diluted earnings per share (EPS) on the face of the statement of operations and requires a reconciliation of the numerators and denominators of basic and diluted EPS calculations. The statement is effective for periods ending after December 15, 1997. The Company has calculated and presented basic and diluted earnings per share on the face of the statement of operations for the years ended December 31, 1997 and 1996 and from the period of February 1995 (inception) to December 31, 1995. Statement of Financial Accounting Standards No. 130 - In June 1997, the Financial Accounting Standards Board (FASB) issued Statement of Financial Accounting Standards No. 130, "Reporting Comprehensive Income," which is required to be adopted for fiscal years beginning after December 15, 1997. This statement establishes standards for reporting and display of comprehensive income and its components in a full set of general-purpose financial statements. This statement requires that all items that are required to be recognized under accounting standards as components of comprehensive income to be reported in a financial statement that is displayed with the same prominence as other financial statements. In the opinion of management, SFAS 130 will not have a material effect on the Company's financial statements. Statement of Financial Accounting Standards No. 131 - In June 1997 the Financial Accounting Standards Board issued Statement of Financial Accounting Standards No. 131, "Disclosures about Segments of an Enterprise and Related Information," effective for fiscal years beginning after December 15, 1997. The statement requires that a public company report financial and descriptive information about its reportable operating segments using the management approach. In the opinion of management, SFAS 131 will not have a material effect on the Company' financial statements. Statement of Position 97-2 - In October 1997, the Accounting Standards Executive Committee issued Statement of Position (SOP) 97-2, "Software Revenue Recognition," which provides guidance on applying generally accepted accounting principles in recognizing revenue on software transactions and is effective for transactions entered into in fiscal years beginning after December 15, 1997. The Company does not believe that the implementation of SOP 97-2 will have a material effect on expected revenues or earnings. 2. AVAILABLE -FOR-SALE SECURITIES The following is a summary of available-for-sale securities as of December 31, 1997: U.S. Government securities $12,232,335 =========== Realized and unrealized gains and losses on available-for-sale securities were immaterial as of and for the year ended December 31, 1997. The cost and estimated fair value of marketable securities by contractual maturity at December 31, 1997 are as follows: Amortized Cost Fair Value ---- ---------- Due in one year or less $ 2,824,280 $ 2,823,704 Due after one year through two years 9,400,389 9,408,631 --------- --------- $12,224,669 $12,232,335 =========== =========== 3. PROPERTY AND EQUIPMENT Property and equipment are summarized as follows at December 31:
1997 1996 ---- ---- Computer software ................................... $ 380,831 $ 307,735 Computer equipment .................................. 600,279 409,681 Telephone equipment ................................. 189,479 134,656 Leasehold improvements .............................. 41,504 37,729 Office furniture and equipment ...................... 249,291 184,708 --------- --------- 1,461,384 1,074,509 Less accumulated depreciation and amortization ...... 502,419 212,472 ------- ------- Property and equipment, net ......................... $ 958,965 $ 862,037 ========== ==========
4. INCOME TAXES The Company has not recorded any income tax expense during the period from Inception to December 31, 1997 because of operating losses incurred since inception As of December 31, 1997, the Company has net operating loss carryforwards for Federal income tax purposes of approximately $7,100,000 which are available to offset future Federal taxable income. These carryforwards expire in varying amounts through 2012. No tax benefit relating to the net operating loss carryforwards has been reflected in the financial statements due to the uncertainty regarding the utilization of any such benefit, and valuation allowances of $2,414,000 for 1997 and $1,326,000 for 1996 have been recognized to offset any deferred tax asset related to these carryforwards. Future benefit may occur to the extent taxable income is earned prior to the expiration of the carryforward period. 5. PUBLIC OFFERING OF COMMON STOCK In December 1996, the Company sold 2,000,000 shares of common stock through an initial public offering which generated net proceeds of $14,082,048 after deducting applicable issuance costs and expenses. On January 8, 1997, an additional 300,000 shares of common stock were sold pursuant to an underwriters over-allotment provision, which generated net proceeds to the Company of $2,232,000 after deducting underwriting discounts and commissions. In connection with this initial public offering, the Company's outstanding shares of Series A and B convertible preferred stock were converted into 2,046,000 shares of common stock. 6. STOCK OPTIONS AND WARRANTS The Company has an Employee Stock Option Plan (the "Stock Option Plan") for the benefit of certain employees, non-employee directors, and key advisors. The Company has adopted the disclosures-only provision of Statement of Financial Accounting Standards No. 123, "Accounting for Stock-Based Compensation". Accordingly, no compensation cost has been recognized for the Stock Option Plan as it relates to employees. Had compensation cost for the Company's stock option plan been determined based on the fair value at the date of grant for awards consistent with the provisions of SFAS No. 123, the Company's net loss and net loss per share would have been increased to the pro forma amounts indicated below:
Period from Feburary 22,1995 Year ended Year ended (Inception) to December 31, 1997 December 31, 1996 December 31, 1995 Net loss - as reported $(3,263,351) $(2,806,43) $(1,116,652) Net loss - pro forma $(3,406,973) $(2,879,457) $(1,125,428) Net loss per share - basic and diluted - as reported $ (0.41) $ (.44) $ (.18) Net loss per share - basic and diluted - pro forma $ (0.43) $ (.46) $ (.18)
The fair value of each option grant is estimated on the date of grant using the Black-Scholes option-pricing model using an assumed risk-free interest rates of 5.98% for the year ended December 31, 1997 and 7% for the year ended December 31, 1996 and an expected life of 7 years. As the Company was still considered a private company for the purposes of applying SFAS No. 123 for the period from Inception to June 30, 1996, the Company did not include a volatility factor assumption in its fair value model. For the options granted after July 1, 1996, the Company has used a volatility factor of .53 for year ended December 31, 1997 and .60 for year ended December 31, 1996. For purposes of pro forma disclosure, the estimated fair value of each option is amortized to expense over that option's vesting period. The Stock Option Plan authorizes 1,080,000 shares of common stock to be issued. Stock options granted under the Stock Option Plan may be of two types: (1) incentive stock options and (2) nonqualified stock options. The option price of such grants shall be determined by a Committee of the Board of Directors (the "Committee"), but shall not be less than the estimated fair market value of the common stock at the date the option is granted. The terms of the grants shall be fixed by the Committee, with no term lasting longer than ten years. The ability to exercise such options shall be determined by the Committee when the options are granted. All of the outstanding options vest at the rate of 20% per year with the exception of 36,000 options which were vested as of the date of grant. A summary of stock option activity follows:
Weighted- Outstanding Average Options Exercise Price ------- -------------- Options granted during the period from Inception to December 31, 1995 (weighted average fair value of $.13) ...................658,800 $ 0.35 Options forfeited by holders during the period from Inception to December 31, 1995 ..........................................(65,520) $ 0.54 Options exercised during the period form Inception to December 31, 1995 ......................................................... (2,880) $ 0.14 ------- Options outstanding at January 1, 1996 .........................................590,400 $ 0.33 Options granted during the year ended December 31, 1996 (weighted average fair value of $3.24) .......................................365,400 $ 5.32 Options forfeited by holders during the year ended December 31, 1996 ......................................................(63,840) $ 0.87 ------- Options outstanding at December 31, 1996 .......................................891,960 $ 2.34 Options granted during the year ended December 31, 1997 (weighted average fair value of $5.16) .......................................307,000 $ 4.39 Options forfeited by holders during the year ended December 31, 1997 .....................................................(342,580) $ 4.83 Options exercised during the year ended December 31, 1997 ......................(58,320) $ 0.22 ------- Options outstanding at December 31, 1997 .......................................798,060 $ 2.21 ======= Options exercisable at December 31, 1997 .......................................212,928 $ 0.82 ======= Options available for grant at December 31, 1997 ...............................281,940 =======
The following table summarizes information concerning outstanding and exercisable options at December 31, 1997:
Options Outstanding Options Exercisable ------------------- ------------------- Weighted Average Weighted Weighted Remaining Average Average Range of Number Contractual Exercise Number Exercise Exercise Price Outstanding Life Price Exercisable Price $.14 - $ .99 390,480 7.36 $ .29 177,792 $ 0.27 $1.00 - $1.99 44,640 7.94 $ 1.57 13,968 $ 1.52 $2.00 - $4.99 272,840 9.24 $ 2.95 13,608 $ 2.08 $5.00 - $10.00 90,100 9.08 $ 8.56 7,560 $10.00 -------- ------- 798,060 212,928 ======= =======
The Company also has outstanding stock purchase warrants entitling the holders to purchase a total of 23,400 shares of common stock at prices ranging from $2.08 to $10.00 per share (weighted average exercise price of $2.69). At December 31, 1997, 4,680 of these warrants are currently vested, with the remaining 18,720 warrants vesting at 20% per year. The Company has recorded compensation cost of $8,283 for the year ended December 31, 1997 and $13,208 for the year ended December 31, 1996 in connection with the issuance of these warrants. 7. COMMITMENTS The Company leases office space for its main operating facility under an operating lease agreement expiring in November 1999. Rental expense from this lease for the years ended December 31, 1997, 1996 and for the period from February 22, 1995 (inception) to December 31, 1995, was $154,907, $70,479 and $40,375 respectively. At December 31, 1997, future minimum lease payments under this lease are summarized as follows: 1998 $180,523 1999 173,100 ------- $353,623 ======== 8. EARNINGS PER SHARE Net loss per share is based on the weighted average number of common shares outstanding subsequent to the Company's initial public offering in 1996.Pursuant to rules of the Securities and Exchange Commission Staff, all common and potential common shares issued by the Company at a price less than the initial public offering price during at least the 12 months preceding the offering date (using the treasury stock method until shares are issued) have been included in the calculation of common and potential common shares outstanding for all periods presented prior to the December 1996 initial public offering. Because th Company is in a loss position at December 31,1997, options to purchase 798,060 shares of common stock at $.14 to $10.00 per share were outstanding as of December 31, 1997 but were not included in the computation of diluted EPS as they would be dilutive. Per Share Net Loss Shares Amount -------- ------ ------ 1997 - ---- Basic and Diluted EPS $(3,263,351) 7,980,094 $(.41) 1996 - ---- Diluted EPS $(2,806,436) 6,347,716 $(.44) 1995 - ---- Diluted EPS $(1,116,652) 5,954,299 $(.18) Item 9. Changes in and Disagreements With Accountants on Accounting and Financial Disclosures. None PART III Item 10. Directors and Executive Officers of the Registrant. Incorporated by reference to the Company's Proxy Statement for Annual Meeting of Stockholders to be filed with the Securities and Exchange Commission within 120 days after the close of the fiscal year ended December 31, 1997. Item 11. Executive Compensation. Director Compensation Incorporated by reference to the Company's Proxy Statement for Annual Meeting of Stockholders to be filed with the Securities and Exchange Commission within 120 days after the close of the fiscal year ended December 31, 1997. Executive Compensation Incorporated by reference to the Company's Proxy Statement for Annual Meeting of Stockholders to be filed with the Securities and Exchange Commission within 120 days after the close of the fiscal year ended December 31, 1997. Item 12. Security Ownership of Certain Beneficial Owners and Management. Incorporated by reference to the Company's Proxy Statement for Annual Meeting of Stockholders to be filed with the Securities and Exchange Commission within 120 days after the close of the fiscal year ended December 31, 1997. Item 13. Certain Relationships and Related Transactions Incorporated by reference to the Company's Proxy Statement for Annual Meeting of Stockholders to be filed with the Securities and Exchange Commission within 120 days after the close of the fiscal year ended December 31, 1997. PART IV Item 14. Exhibits, Financial Statement Schedules and Reports on Form 8-K (a) Financial Statements: The financial statements of the Company are included in Part II, Item 8. (b) Reports on Form 8 - K: No reports on Form 8-K were filed during the fourth quarter of the year ended December 31, 1997. ( c) Exhibits: Exhibit # Description of Exhibits (3) Articles of Incorporation and By-Laws: Certificate of Incorporation Incorporated herein by reference from Exhibit 3.1 on Form S-1 Registration Statement of the Company, filed with the Commission on December 17, 1996. By-Laws Incorporated herein by reference from Exhibit 3.3 on Form S-1 Registration Statement of the Company, filed with the Commission on December 17, 1996. (10) Material contracts: 10.1 Employment agreement with Donald A. Carlberg, President and Chief Executive Officer, dated March 1, 1995, incorporated by reference from Exhibit 10.1 on Form S-1 Registration Statement of the Company, filed with the Commission on December 17, 1996. 10.2 Patient Infosystems, Inc. Stock Option Plan, incorporated by reference from Exhibit 10.2 on Form S-1 Registration Statement of the Company, filed with the Commission on December 17, 1996. 10.3 Patient Infosystems, Inc. Stock Option Agreement, incorporated by reference from Exhibit 10.3 on Form S-1 Registration Statement of the Company, filed with the Commission on December 17, 1996. 10.4 Services Agreement dated September 18, 1995 between the Company and Bristol-Myers Squibb U.S. Pharmaceuticals, a division of Bristol-Myers Squibb Company, incorporated by reference from Exhibit 10.4 on Form S-1 Registration Statement of the Company, filed with the Commission on December 17, 1996. 10.5 Services Agreement dated February 1, 1996 between the Company and Bristol-Myers Squibb U.S. Pharmaceuticals, a division of Bristol-Myers Squibb Company, incorporated by reference from Exhibit 10.5 on Form S-1 Registration Statement of the Company, filed with the Commission on December 17, 1996. 10.6 Services Agreement dated March 30, 1996 between the Company and Bristol-Myers Squibb Oncology, a division of Bristol-Myers Squibb Company, incorporated by reference from Exhibit 10.6 on Form S-1 Registration Statement of the Company, filed with the Commission on December 17, 1996. 10.7 Services Agreement dated April 23, 1996 between the Company and Bristol-Myers Squibb Oncology/Immunology, a division of Bristol-Myers Squibb Company, incorporated by reference from Exhibit 10.7 on Form S-1 Registration Statement of the Company, filed with the Commission on December 17, 1996. 10.8 Services Agreement dated October 16, 1995 between the Company and Bristol-Myers Squibb U.S. Pharmaceuticals, a division of Bristol-Myers Squibb Company, incorporated by reference from Exhibit 10.8 on Form S-1 Registration Statement of the Company, filed with the Commission on December 17, 1996. 10.9 Services Agreement dated June 24, 1996 between the Company and American HomePatient, Inc., incorporated by reference from Exhibit 10.9 on Form S-1 Registration Statement of the Company, filed with the Commission on December 17, 1996. 10.10 Services Agreement dated June 21, 1996 between the Company and Equifax Healthcare Administrative Services, a division of Equifax, Inc., incorporated by reference from Exhibit 10.10 on Form S-1 Registration Statement of the Company, filed with the Commission on December 17, 1996. 10.11 Services Agreement dated July 28, 1996 between the Company and Equifax Healthcare Administrative Services, a division of Equifax, Inc., incorporated by reference from Exhibit 10.11 on Form S-1 Registration Statement of the Company, filed with the Commission on December 17, 1996. 10.12 Services Agreement dated September 13, 1996 between the Company and Health Resources, Inc.(Asthma), incorporated by reference from Exhibit 10.12 on Form S-1 Registration Statement of the Company, filed with the Commission on December 17, 1996. 10.13 Services Agreement dated September 13, 1996 between the Company and Health Resources Inc.(Diabetes), incorporated by reference from Exhibit 10.13 on Form S-1 Registration Statement of the Company, filed with the Commission on December 17, 1996. 10.14 Services Agreement dated September 13, 1996 between the Company and Harris Methodist Health Plan, incorporated by reference from Exhibit 10.14 on Form S-1 Registration Statement of the Company, filed with the Commission on December 17, 1996. (11) Statement of Computation of Per Share Earnings See page 38 of this Annual report on Form 10-K. (27) Financial Data Schedule Filed electronically All other exhibits are omitted because they are not applicable or the required information is shown elsewhere in this Annual Report on Form 10-K. EX-11 2 COMPUTATION OF PER SHARE EARNINGS Exhibit 11. Statement of Computation of Per Share Earnings.
PATIENT INFOSYSTEMS, INC. COMPUTATION OF EARNINGS PER SHARE Period From February 22, 1995 Year Ended Year Ended (Inception) to December 31, December 31, December 31, 1997 1996 1995 ---- ---- ---- Net Loss ............................................... $(3,263,351) $(2,806,436) $(1,116,652) Weighted average Common Stock outstanding .............. 7,980,094 3,678,435 3,602,880 Weighted average Series A Convertible Preferred Stock... outstanding............................................. - 1,296,000 518,400 Weighted average Series B Convertible Preferred Stock outstanding ............................................ - 437,500 - Staff Accounting Bulletin Common Stock Equivalents: Series A Convertible Preferred Stock issued August and September 1995, calculated using the treasury stock method .......................................... - - 642,600 Series B Convertible Preferred Stock issued May and June 1996, calculated using the treasury stock method ................................................ - 177,365 375,000 Dilutive effect of stock options granted in the preceding twelve months, calculated using the treasury stock method ................................. - 758,416 815,419 Weighted average common and potential common shares ....................................... 7,980,094 6,347,716 5,954,299 Net Loss per share - Basic and Diluted .................. $ (.41) $ (.44) $ (.18) =========== =========== ===========
Pursuant to the requirements of Section 13 or 15(d) of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized. PATIENT INFOSYSTEMS, INC. By: /s/ Donald A. Carlberg Donald A. Carlberg Director, President, and Chief Executive Officer Pursuant to the requirements the Securities and Exchange Act of 1934, this report has been signed below by the following persons on behalf of the registrant and in the capacities and on the dates indicated. By: /s/ Donald A. Carlberg March 31, 1998 Donald A. Carlberg Date Director, President and Chief Executive Officer By: /s/ Derace L. Schaffer, M.D. March 31, 1998 Derace L. Schaffer, M.D Date Chairman of the Board By: /s/ John Pappajohn March 31, 1998 John Pappajohn Date Director By: /s/ Barbara J. McNeil, M.D., Ph.D March 31 ,1998 Barbara J. McNeil, M.D., Ph.D. Date Director By: /s/ Carl F. Kohrt, Ph.D. March 31 , 1998 Carl F. Kohrt, Ph.D. Date Director EX-27 3 FINANCIAL DATA SCHEDULE
5 1 YEAR DEC-31-1997 JAN-01-1997 DEC-31-1997 779,317 12,232,335 412,956 0 0 13,830,115 1,461,384 502,419 15,036,473 587,728 0 0 0 80,115 14,368,630 15,036,473 2,062,373 2,062,373 1,629,128 6,160,840 0 0 0 (3,263,351) 0 (3,263,351) 0 0 0 (3,263,351) (0.41) (0.41)
-----END PRIVACY-ENHANCED MESSAGE-----