Item 1A. Risk Factors
ITEM 1A – RISK FACTORS
You should carefully consider the risks described
below, as well as the other information in this Annual Report on Form 10-K, including our financial statements and the related notes and
the section entitled “Management’s Discussion and Analysis of Financial Condition and Results of Operations,” before
investing in our publicly traded securities. The occurrence of any of the events or developments described below could harm our business,
financial condition, operating results, and/or growth prospects. The risks described below are not the only ones facing us. Our business
is also subject to the risks that affect many other companies, such as competition, technological obsolescence, labor relations, general
economic conditions, geopolitical changes, and international operations. We operate in a rapidly changing environment that involves a
number of risks, some of which are beyond our control. Additional risks not currently known to us or that we currently believe are immaterial
also may impair our business operations and our liquidity. The risks described below could cause our actual results to differ materially
from those contained in the forward-looking statements we have made in this Annual Report on Form 10-K, the information incorporated herein
by reference, and those forward-looking statements we may make from time to time. You should understand that it is not possible to predict
or identify all such factors. Consequently, you should not consider the following to be a complete discussion of all potential risks or
uncertainties.
Risk Factor Summary
Below is a summary of the principal factors
that make an investment in our common stock speculative or risky. This summary does not address all of the risks that we face. Additional
discussion of the risks summarized in this risk factor summary, and other risks that we face, can be found below and should be carefully
considered, together with other information included in this prospectus.
·
Our business is subject to risks arising from epidemic diseases, such as the recent outbreak of the COVID-19 illness.
·
Our ability to sustain or increase revenues will depend upon our success in entering new markets, continuing to increase our customer base, and in deriving additional revenues from our existing customers.
·
Consolidation and increasing competition within the pharmaceutical and biotechnology industries ,
drug development and services industry, and the life science market for modeling and simulation software and for cheminformatics products
may decrease the number of our customers and/or affect demand for our products and services.
·
Increasing competition and increasing costs
within the pharmaceutical and biotechnology industries may affect the demand for our products and services, which may affect our results
of operations and financial condition.
·
Health care reform and restrictions on reimbursement may affect the companies that purchase or license our products or services, which may affect our results of operations and financial condition.
·
We face strong competition in the life science
market for modeling and simulation software and for cheminformatics products.
·
We are subject to pricing pressures in some of the markets we serve.
·
Our operations may be interrupted by the
occurrence of a natural disaster or other catastrophic event at our primary facilities.
·
Our insurance coverage may not be sufficient to avoid material impact on our financial position or results of operations resulting from claims or liabilities against us, and we may not be able to obtain insurance coverage in the future.
·
Changes in government regulation or in practices relating to the pharmaceutical or biotechnology industries could decrease the need for the services we provide.
·
Any negative commentaries made by any regulatory agencies or any failure by us to comply with applicable regulations
and related guidance could harm our reputation and operating results, and compliance with new regulations and guidance may result in additional
costs.
·
Our sales cycle is lengthy and customers may delay entering into contracts or decide not to adopt our products or
solutions after we have expended significant time and resources and supported evaluation by them of our technology, which could result
in delays in recognizing revenue and negatively impact our results of operations.
·
Many of our contracts are fixed-price and may be delayed or terminated or reduced in scope for reasons beyond our control, or we may underprice or overrun cost estimates with these contracts, potentially resulting in financial losses.
·
We could experience a breach of the confidentiality
of the information we hold or of the security of our computer systems.
·
Impairment of goodwill or intangible assets may adversely impact future results of operations.
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·
Software defects or malfunctions in our products could hurt our reputation among our customers, result in delayed or lost revenue, and expose us to liability.
·
Delays in the release of new or enhanced products or services or undetected errors in our products or services may result in increased cost to us, delayed market acceptance of our products, and delayed or lost revenue.
·
We are subject to risks associated with the operation of a global business.
·
The drug discovery and development services industry is highly competitive.
·
Changes in applicable U.S. and international tax laws or regulations and the resolution of tax disputes could negatively affect our financial results.
·
Contract research services create a risk of liability.
·
Upgrading our software could result in implementation issues and business disruptions.
·
The drug discovery and development industry has a history of patent and other intellectual property litigation, and we might be involved in costly intellectual property lawsuits.
·
We may not be able to successfully develop and market new services and products.
·
Ability to incur debt could adversely affect our business and growth prospects.
·
We depend on key personnel and may not be able to retain these employees or recruit additional qualified personnel, which could harm our business.
·
If we are not successful in selecting and integrating the businesses and technologies we acquire, or in managing our current and future divestitures, our business may suffer.
·
Our quarterly and annual operating results fluctuate and may continue to fluctuate in the future, and if we fail
to meet the expectations of analysts or investors, our stock price and the value of your investment could decline substantially.
·
We derive a significant percentage of our revenues from a concentrated group of customers and the loss of more than
one of our major customers could materially and adversely affect our business, results of operations or financial condition.
·
We conduct business outside the U.S., which exposes us to foreign currency exchange rate risk, amongst other risk,
and could have a negative impact on our financial results.
·
A significant portion of our operating expenses is relatively fixed and planned expenditures are based in part
on expectations regarding future revenues.
·
If our customers cancel their contracts or terminate or delay their clinical trials, we may lose or delay revenues
and our business may be harmed.
·
If our security is breached, our business could be disrupted, our operating results could be harmed, and customers
could be deterred from using our products and services.
·
Any failure by us to properly protect customer data we possess or are deemed to possess, in connection with the conduct
of clinical trials, could subject us to significant liability.
·
We rely upon a single internal hosting facility and Amazon Web Services to deliver our solutions to our customers
and any disruption of or interference with our hosting systems, operations, or use of the Amazon Web Services could harm our business
and results of operations.
·
Defects or errors in our software applications could harm our reputation, result in significant cost to us and impair
our ability to market our solutions.
·
If we are not able to reliably meet our data storage and management requirements, or if we experience any failure
or interruption in the delivery of our services over the Internet, customer satisfaction and our reputation could be harmed and customer
contracts may be terminated.
·
Some of our software solutions and services utilize open source software, and any failure to comply with the terms
of one or more of these open source licenses could adversely affect our business.
·
We may be unable to adequately enforce or defend our ownership and use of our intellectual property and other proprietary
rights.
·
Current and future litigation against us, which may arise in the ordinary course of our business, could be costly and
time-consuming to defend.
·
We could incur substantial costs resulting from product liability claims relating to our products or services or
our customers’ use of our products or services.
·
Our business depends on the clinical trial market, and a downturn in this market could cause our revenues to decrease.
·
As a public company, we are obligated to maintain proper and effective internal control over financial reporting.
As our business expands both organically and through acquisitions, we may be unable to effectively adapt our current systems to our changing
business needs and may fail to develop and maintain an effective system of disclosure controls and internal control over financial reporting
which could impair our ability to produce timely and accurate financial statements or comply with applicable laws and regulations.
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·
As a public company, we may incur significant administrative workload and expenses in connection with new and changing
compliance requirements.
·
We have been paying quarterly dividends on shares of our common stock, and although there has been a consistent
track record of paying these dividends, the Board of Directors may suspend the dividend, and, consequently, your ability to achieve a
return on your investment will depend on appreciation in the price of our common stock.
·
If our operating and financial performance in any given period does not meet any guidance that we provide to the
public, the market price of our common stock may decline.
·
The price of our common stock may fluctuate significantly, and investors could lose all or part of their investments.
·
The price of our common stock may be volatile, and our stockholders may not be able to resell shares of our common
stock at or above the price they paid.
·
If securities or industry analysts issue an adverse or misleading opinion regarding our stock, or our inclusion
in the S&P 600 discontinues, our stock price and trading volume could decline.
·
We may raise capital through the issuance of our common stock, convertible debt or equity linked securities, which
could result in dilution to our stockholders or negatively impact the price of our common stock.
Certain Risks Related to Our Business
Our business is subject to risks arising
from epidemic diseases, such as the recent outbreak of the COVID-19 illness.
We
are subject to risks related to public health crises such as the global pandemic associated with COVID-19. In December 2019, a novel
strain of coronavirus, SARS-CoV-2, was reported to have surfaced in Wuhan, China. Since then, COVID-19 has spread worldwide and has
resulted in government authorities implementing numerous measures to try to contain it, such as travel bans and restrictions,
quarantines, shelter-in-place orders and shutdowns. The ongoing COVID-19 global pandemic and variants thereof is having widespread,
rapidly-evolving, and unpredictable impacts on global societies, economies, financial markets, and business practices. COVID-19
poses the risk that we or our employees, contractors, suppliers, and other partners may be prevented from conducting business
activities for an indefinite period of time, including due to shutdowns that may be requested or mandated by governmental
authorities. If the current economic conditions worsen or last for an extended period of time, we may be forced to significantly
scale back our business and growth plans, which could have a material adverse effect on our business.
We have undertaken several measures in an effort
to mitigate the spread of COVID-19, including adjusting our business practices to combat the effects by restricting employee travel, closing
our offices in compliance with local guidelines and, when reopened, implementing social distancing at our office locations and additional
sanitary measures. There have been no reductions in our workforce as a result of COVID-19. During the 2021 fiscal year, software renewal
revenue and services revenues generated primarily from contracts signed prior to the effects of the pandemic have not been materially
impacted. Revenue from new software licenses and new service contracts has been negatively impacted with our clients’ increased
focus on opportunities to address COVID-19 mitigation efforts and disruption in drug programs in other therapeutic areas.
While the COVID-19 pandemic has not materially
adversely affected our business operations as of the date of this Annual Report on Form 10-K, the continued spread of COVID-19 and variants
thereof and the measures taken by the governments of countries affected could disrupt the supply chain and adversely impact our business,
financial condition, or results of operations. The COVID-19 outbreak and mitigation measures may also continue to have an adverse impact
on global economic conditions, which could have an adverse effect on our business and financial condition. The extent to which the COVID-19
outbreak further impacts our results going forward will depend on future developments that are highly uncertain and cannot be predicted,
including but not limited to, the continued duration and spread of the outbreak, the emergence of novel variants, the degree of severity
of the outbreak and existing and new variants, the development and administration of existing and new therapeutic treatments and vaccines,
the actions taken by national, regional, and local governments and health officials to contain the virus or treat its impact, how quickly
and to what extent normal economic and operating conditions can resume, and the extent to which our third-party partners and/or customers
experience any business interruptions as a result thereof. In addition, a recession or market correction resulting from the spread of
COVID-19 could materially affect our business and the value of our common stock.
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Certain Risks Related to Our Marketplace and
Environment
Our ability to sustain or increase revenues
will depend upon our success in entering new markets, continuing to increase our customer base, and in deriving additional revenues from
our existing customers.
Our products are currently used primarily by modeling
and simulation specialists in pharmaceutical, biotechnology, agrotechnology, cosmetics, and government research organizations. One component
of our overall business strategy is to derive more revenues from our existing customers by expanding their use of our products and services.
Such strategy would have our customers utilize our scientific informatics platforms and our tools and components to leverage vast amounts
of information stored in both corporate databases and public data sources in order to make informed scientific and business decisions
during the research and development process. In addition, we seek to expand into new markets, and new areas within our existing markets,
by acquiring businesses in these markets, attracting and retaining personnel knowledgeable in these markets, identifying the needs of
these markets, and developing marketing programs to address these needs. If successfully implemented, these strategies would increase
the usage of our software and services by pharmacologists or pharmacometricians operating within our existing pharmaceutical, biotechnology,
and chemical customers, as well as by new customers in other industries. However, if our strategies are not successfully implemented,
our products and services may not achieve market acceptance or penetration in targeted new departments within our existing customers or
in new industries. As a result, we may incur additional costs and expend additional resources without being able to sustain or increase
revenue.
Consolidation within the pharmaceutical
and biotechnology industries may continue to lead to fewer potential customers for our products and services .
A significant portion of our customer base consists
of pharmaceutical and biotechnology companies. Consolidation within the pharmaceutical and biotechnology industries may result in fewer
customers for our products and services. Although the industry consolidation that has taken place over the past 20 years has not prevented
our business from growing to date, if one of the parties to a consolidation uses the products or services of our competitors, we may lose
existing customers as a result of such consolidation.
Increasing competition and increasing costs
within the pharmaceutical and biotechnology industries, drug development and services industry, and the life science market for modeling
and simulation software and for cheminformatics products may affect the demand for our products and services, which may affect our results
of operations and financial condition .
Our pharmaceutical and biotechnology customers’
demand for our products is impacted by continued demand for their products and by our customers’ research and development costs.
Demand for our customers’ products could decline, and prices charged by our customers for their products may decline, as a result
of increasing competition, including competition from companies manufacturing generic drugs. In addition, our customers’ expenses
could continue to increase as a result of increasing costs of complying with government regulations and other factors. A decrease in demand
for our customers’ products, pricing pressures associated with the sales of these products, and additional costs associated with
product development, could cause our customers to reduce research and development expenditures. Although our products increase productivity
and reduce costs in many areas, because our products and services depend on such research and development expenditures, our revenues may
be significantly reduced.
Health care reform and restrictions on reimbursement
may affect the pharmaceutical, biotechnology, and industrial chemical companies that purchase or license our products or services, which
may affect our results of operations and financial condition .
The continuing efforts of government and third-party
payers in the markets we serve to contain or reduce the cost of health care may reduce the profitability of pharmaceutical, biotechnology,
and industrial chemical companies, causing them to reduce research and development expenditures. Because some of our products and services
depend on such research and development expenditures, our revenues may be significantly reduced. We cannot predict what actions federal,
state, or private payers for health care goods and services may take in response to any health care reform proposals or legislation.
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We face strong competition in the life science
market for modeling and simulation software and for cheminformatics products.
The market for our modeling and simulation software
products for the life science market is intensely competitive. We currently face competition from other scientific software providers,
larger technology and solutions companies, in-house development by our customers and academic and government institutions, and the open-source
community. Some of our competitors and potential competitors have longer operating histories in certain segments of our industry than
we do and could have greater financial, technical, marketing, research and development, and other resources. Many of our competitors offer
products and services directed at more specific markets than those we target, enabling these competitors to focus a greater proportion
of their efforts and resources on these markets. Some offerings that compete with our products are developed and made available at lower
cost by government organizations and academic institutions, and these entities may be able to devote substantial resources to product
development and also offer their products to users for little or no charge. We also face competition from open-source software initiatives,
in which developers provide software and intellectual property free over the Internet. In addition, some of our customers spend significant
internal resources in order to develop their own software. Moreover, we intend to leverage our scientific informatics platform in order
to enable our customers to more effectively utilize the vast amounts of information stored in both their databases and public data sources
in order to make informed scientific and business decisions during the research and development process. This strategy could lead to competition
from much larger companies that provide general data storage and management software. There can be no assurance that our current or potential
competitors will not develop products, services, or technologies that are comparable to, superior to, or render obsolete, the products,
services, and technologies we offer. There can be no assurance that our competitors will not adapt more quickly than we to technological
advances and customer demands, thereby increasing such competitors’ market share relative to ours. Any material decrease in demand
for our technologies or services may have a material adverse effect on our business, financial condition, and results of operations.
We are subject to pricing pressures in some
of the markets we serve.
The market for modeling and simulation products
for the life science industry is intensely competitive. Although the average price of our software licenses has increased or remained
relatively constant for fiscal years 2019, 2020, and 2021, we may experience a decline in the future. In response to increased competition
and general adverse economic conditions in this market, we may be required to modify our pricing practices. Changes in our pricing model
could adversely affect our revenues and earnings.
Our operations may be interrupted by the
occurrence of a natural disaster or other catastrophic event at our primary facilities.
Our research and development operations and administrative
functions are primarily conducted at our facilities in Lancaster, California, Buffalo, New York, Paris, France and Research Triangle Park,
North Carolina. Although we have contingency plans in effect for natural disasters or other catastrophic events, the occurrence of such
events could still disrupt our operations. For example, our Lancaster, California facility is located in a state that is particularly
susceptible to earthquakes. Any natural disaster or catastrophic event in our facilities or the areas in which they are located could
have a significant negative impact on our operations.
Our insurance coverage may not be sufficient
to avoid material impact on our financial position or results of operations resulting from claims or liabilities against us, and we may
not be able to obtain insurance coverage in the future.
We maintain insurance coverage for protection
against many risks of liability. The extent of our insurance coverage is under continuous review and is modified as we deem it necessary.
Despite this insurance, it is possible that claims or liabilities against us may have a material adverse impact on our financial position
or results of operations. In addition, we may not be able to obtain any insurance coverage, or adequate insurance coverage, when our existing
insurance coverage expires. For example, we do not carry earthquake insurance for our facilities in Lancaster, California, because we
do not believe the costs of such insurance are reasonable in relation to the potential risk for our part of California.
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Changes in government regulation or in practices
relating to the pharmaceutical or biotechnology industries, including potential health care reform, could decrease the need for the services
we provide.
Governmental agencies throughout the world, but
particularly in the U.S., strictly regulate the drug development process. Our business involves helping pharmaceutical and biotechnology
companies, among others, navigate the regulatory drug approval process. Accordingly, many regulations, and often new regulations, are
expected to result in higher regulatory standards and often additional revenues for companies that service these industries. However,
some changes in regulations, such as a relaxation in regulatory requirements or the introduction of streamlined or expedited drug approval
procedures, or an increase in regulatory requirements that we have difficulty satisfying or that make our services less competitive, could
eliminate or substantially reduce the demand for our services.
Any negative commentaries made by any regulatory
agencies or any failure by us to comply with applicable regulations and related guidance could harm our reputation and operating results,
and compliance with new regulations and guidance may result in additional costs.
Any negative commentaries made by any regulatory
agencies or any failure on our part to comply with applicable regulations could result in the termination of ongoing research or the disqualification
of data for submission to regulatory authorities. This could harm our reputation, our prospects for future work, and our operating results.
If our operations are found to violate any applicable law or other governmental regulations, we might be subject to civil and criminal
penalties, damages, and fines. Any action against us for violation of these laws, even if we successfully defend against it, could cause
us to incur significant legal expenses, divert our management’s attention from the operation of our business, and damage our reputation.
Our sales cycle is lengthy and customers
may delay entering into contracts or decide not to adopt our products or solutions after we have expended significant time and resources
and supported evaluation by them of our technology, which could result in delays in recognizing revenue and negatively impact our results
of operations.
On-going negotiations and evaluation projects
for new products, with new customers or in new markets may not result in significant revenues for us if we are unable to close new engagements
on terms favorable to us, in a timely manner, or at all. Unexpected delays in our sales cycle could cause our revenues to fall short of
expectations. Further, the timing and length of negotiations required to enter into agreements with our customers and the ultimate enforcement
of complex negotiated contractual provisions as we intended is difficult to predict. If we do not successfully negotiate certain key complex
contractual provisions, there are disputes regarding such provisions, or they are not enforceable as we intended, our revenues and results
of operations would suffer. Further, if we were to incur significant effort and then fail to enter into final contracts with prospective
customers, or if a contract is terminated earlier than expected, our revenues and results of operations could suffer.
Many of our contracts are fixed-price and
may be delayed or terminated or reduced in scope for reasons beyond our control, or we may underprice or overrun cost estimates with these
contracts, potentially resulting in financial losses.
Many of our contracts provide for services on
a fixed-price or fee-for-service with a cap basis and, accordingly, we bear the financial risk if we initially underprice our contracts
or otherwise overrun our cost estimates. In addition, these contracts may be terminated or reduced in scope either immediately or upon
notice. Cancellations may occur for a variety of reasons, and often at the discretion of the client. The loss, reduction in scope, or
delay of a large contract or the loss or delay of multiple contracts could materially adversely affect our business, although our contracts
frequently entitle us to receive the costs of winding down the terminated projects, as well as all fees earned by us up to the time of
termination. Some contracts also entitle us to a predetermined termination fee and irrevocably committed costs/expenses.
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We could experience a breach of the confidentiality
of the information we hold or of the security of our computer systems.
We operate large and complex computer systems
that contain significant amounts of client data. As a routine element of our business, we collect, analyze, and retain substantial amounts
of data pertaining to the clinical study data analysis we conduct for our clients. Unauthorized third parties could attempt to gain entry
to such computer systems for the purpose of stealing data or disrupting the systems. We believe that we have taken appropriate measures
to protect them from intrusion, and we continue to improve and enhance our systems in this regard, but in the event that our efforts are
unsuccessful, we could suffer significant harm. Our contracts with our clients typically contain provisions that require us to keep confidential
the information generated from these studies. In the event the confidentiality of such information was compromised, we could suffer significant
harm.
Impairment of goodwill or intangible assets
may adversely impact future results of operations.
We have intangible assets, including goodwill,
capitalized computer software development costs, intellectual property, and other intangible assets, on our balance sheet due to our acquisitions
of businesses. The initial identification and valuation of these intangible assets and the determination of the estimated useful lives
at the time of acquisition involve use of management judgments and estimates. These estimates are based on, among other factors, input
from accredited valuation consultants, reviews of projected future income cash flows, and statutory regulations. The use of alternative
estimates and assumptions might have increased or decreased the estimated fair value of our goodwill and intangible assets that could
potentially result in a different impact to our results of operations. If the future growth and operating results of our business are
not as strong as anticipated and/or our market capitalization declines, this could impact the assumptions used in calculating the fair
value of goodwill or intangibles. To the extent goodwill or intangibles are impaired, their carrying value will be written down to its
implied fair value and a charge will be made to our income from continuing operations. Such an impairment charge could materially and
adversely affect our operating results. As of August 31, 2021, and 2020, the carrying amount of goodwill and intangibles was
$37.5 and $37.9 million, respectively, on our consolidated balance sheet.
Certain Risks Related to Our Operations
Software defects or malfunctions in our
products could hurt our reputation among our customers, result in delayed or lost revenue, and expose us to liability.
Our business and the level of customer acceptance
of our products depend upon the continuous, effective, and reliable operation of our software and related tools and functions. To the
extent that defects cause our software to malfunction and our customers’ use of our products is interrupted, our reputation could
suffer and our revenue could decline or be delayed while such defects are remedied. We may also be subject to liability for the defects
and malfunctions of third-party technology partners and others with whom our products and services are integrated.
Delays in the release of new or enhanced
products or services or undetected errors in our products or services may result in increased cost to us, delayed market acceptance of
our products, and delayed or lost revenue.
To achieve market acceptance, new or enhanced
products or services can require long development and testing periods, which may result in delays in scheduled introduction. Any delays
in the release schedule for new or enhanced products or services may delay market acceptance of these products or services and may result
in delays in new customer orders for these new or enhanced products or services or the loss of customer orders. In addition, new or enhanced
products or services may contain a number of undetected errors or “bugs” when they are first released. Although we extensively
test each new or enhanced software product or service before it is released to the market, there can be no assurance that significant
errors will not be found in existing or future releases. As a result, in the months following the introduction of certain releases, we
may need to devote significant resources to correct these errors. There can be no assurance, however, that all of these errors can be
corrected.
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We are subject to risks associated with
the operation of a global business.
We derive a significant portion of our total revenue
from our operations in international markets. During the years ended August 31, 2021, 2020 and 2019, 31%, 29% and 34% respectively, of
our total revenue was derived from our international operations. Our global business may be affected by local economic conditions, including
inflation, recession, and currency exchange rate fluctuations. In addition, political and economic changes, including international conflicts
and terrorist acts, throughout the world may interfere with our or our customers’ activities in particular locations and result
in a material adverse effect on our business, financial condition, and operating results. Potential trade restrictions, exchange controls,
adverse tax consequences, and legal restrictions may affect the repatriation of funds into the U.S. Also, we could be subject to unexpected
changes in regulatory requirements, the continued global spread and impact of the COVID-19 pandemic, the difficulties of compliance with
a wide variety of foreign laws and regulations, potentially negative consequences from changes in or interpretations of U.S. and foreign
tax laws, import and export licensing requirements, and longer accounts receivable cycles in certain foreign countries. These risks, individually
or in the aggregate, could have an adverse effect on our results of operations and financial condition. For example, we are subject to
compliance with the U.S. Foreign Corrupt Practices Act and similar anti-bribery laws, which generally prohibit companies and their intermediaries
from making improper payments to foreign government officials for the purpose of obtaining or retaining business. While our employees,
distributors, and agents are required to comply with these laws, we cannot be sure that our internal policies and procedures will always
protect us from violations of these laws despite our commitment to legal compliance and corporate ethics. The occurrence or allegation
of these types of risks may adversely affect our business, performance, prospects, value, financial condition, and results of operations.
The drug discovery and development services
industry is highly competitive.
Our clinical pharmacology division often competes
for business not only with other clinical research organization (“CROs”), but also with internal discovery and development
departments within our larger clients, who may have greater resources than ours. We also compete with universities and teaching hospitals
for outsourced services. We compete based on a variety of factors, including without limitation:
·
reputation for on-time quality performance;
·
reputation for regulatory compliance;
·
expertise and experience in multiple specialized areas;
·
scope and breadth of service and product offerings across the drug discovery and development spectrum;
·
ability to provide flexible and customized solutions to support our clients’ drug discovery and development needs;
·
price/value;
·
technological expertise and efficient drug development processes;
·
financial stability;
·
accessibility of client data through secure portals; and
·
ability to acquire, process, analyze, and report data in an accurate manner.
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If we do not compete successfully, our business
could suffer. Increased competition could lead to price and other concessions that might adversely affect our operating results. The drug
discovery and development services industry has continued to see a trend towards consolidation, particularly among biotechnology companies,
who are acquisition targets for each other and for larger pharmaceutical companies. If this trend continues, it is likely to produce more
competition among the larger companies and CROs generally, with respect to both clients and acquisition candidates. In addition, while
there are substantial barriers to entry for large, global competitors with broad-based services, small, specialized entities considering
entering the CRO industry will continue to find lower barriers to entry, and private equity firms may determine that there are opportunities
to acquire and consolidate these companies, thus further increasing possible competition. More generally, our competitors or others might
develop technologies, services, or products that are more effective or commercially attractive than our current or future technologies,
services, or products, or that render our technologies, services, or products less competitive or obsolete. If competitors introduce superior
technologies, services, or products and we cannot make enhancements to ours to remain competitive, our competitive position, and in turn
our business, revenue, and financial condition, would be materially and adversely affected. In the aggregate, these competitive pressures
may affect the attractiveness of our technologies, services, or products and could adversely affect our financial results.
Changes in applicable U.S. and international
tax laws or regulations and the resolution of tax disputes could negatively affect our financial results.
We are subject to income taxes, as well as non-income-based
taxes, in both the U.S. and various foreign jurisdictions in which we do business. Significant judgment is required in determining our
worldwide provision for income taxes and other tax liabilities. Changes in tax laws or tax rulings may have a significant adverse impact
on our effective tax rate. For example, the U.S. and many countries where we do business are actively considering or have recently enacted
changes in relevant tax, accounting and other laws, regulations and interpretations. Recently, the Biden Administration committed to increasing
the corporate income tax rate, and to increasing the tax rate applied to profits earned outside the U.S. If enacted, the impact of these
potential new rules could be material to our tax provision and value of deferred tax assets and liabilities.
Further, in the ordinary course of a global business,
there are many intercompany transactions and calculations where the ultimate tax determination could change if tax laws or tax rulings
were to be modified. We are also subject to non-income-based taxes, such as payroll, sales, use, value-added, net worth, property and
goods and services taxes, in both the U.S. and various foreign jurisdictions. Although we believe that our income and non-income-based
tax estimates are appropriate, there is no assurance that the final determination of tax audits or tax disputes will not be different
from what is reflected in our historical income tax provisions and accruals.
Given the unpredictability of possible further
changes to the U.S. or foreign tax laws and regulations and their potential interdependency, it is very difficult to predict the cumulative
effect of such tax laws and regulations on our results of operations and cash flow, but such laws and regulations (and changes thereto)
could adversely impact our financial results.
Contract research services create a risk of liability.
As a CRO, we face a range of potential liabilities which may include:
·
Errors or omissions in reporting of study detail in preclinical studies that may lead to inaccurate reports, which may undermine the usefulness of a study or data from the study, or which may potentially advance studies absent the necessary support or inhibit studies from proceeding to the next level of testing; and
·
Risks associated with our possible failure to properly care for our clients’ property, such as research models, records, work in progress, or other archived materials.
Contractual risk transfer indemnifications generally
do not protect us against liability arising from certain of our own actions, such as negligence or misconduct. We could be materially
and adversely affected if we are required to pay damages or bear the costs of defending any claim that is outside any contractual indemnification
provision, or if a party does not fulfill its indemnification obligations, or the damage is beyond the scope or level of insurance coverage.
We also often contractually indemnify our clients (subject to a limitation of liability), similar to the way they indemnify us, and we
may be materially adversely affected if we have to fulfill our indemnity obligations. Furthermore, there can be no assurance that we nor
a party required to indemnify us will be able to maintain such insurance coverage (either at all or on terms acceptable to us).
22
Upgrading our software could result in implementation
issues and business disruptions.
We update our software on a regular basis and
are continually in the process of refactoring our software programs. In doing so, we face the possibility that existing users will find
the software unacceptable, or new users may not be as interested as they have been in the past versions. Translation errors might introduce
new software bugs that will not be caught.
The drug discovery and development industry
has a history of patent and other intellectual property litigation, and we might be involved in costly intellectual property lawsuits.
The drug discovery and development industry has
a history of patent and other intellectual property litigation and these lawsuits will likely continue. Accordingly, we face potential
patent infringement suits by companies that have patents for similar products and methods used in business or other suits alleging infringement
of their intellectual property rights. Legal proceedings relating to intellectual property could be expensive, take significant time,
and divert management’s attention from other business concerns, whether we win or lose. If we do not prevail in an infringement
lawsuit brought against us, we might have to pay substantial damages, including treble damages, and we could be required to stop the infringing
activity or obtain a license to use technology on unfavorable terms.
We may not be able to successfully develop
and market new services and products.
We may seek to develop and market new services
and products that complement or expand our existing business or service offerings. We cannot guarantee that we will be able to identify
new technologies of interest to our customers. Even if we are able to identify new technologies of interest, we may not be able to negotiate
license agreements on acceptable terms, or at all. If we are unable to develop new services and products and/or create demand for those
newly developed services and products, our future business, results of operations, financial condition, and cash flows could be adversely
affected.
Ability to incur debt could adversely affect our business and
growth prospects.
On March 31, 2020 we established a line of credit
with a bank in the amount of $3,500,000 and, to date, we have not accessed the line. Prior to the establishment of the line we have not
had any borrowed debt and have no need to do so to fund normal operations in the foreseeable future. Should circumstances require us to
incur additional debt and a lender could not be found to provide that debt, this could have a significant adverse effect on our business,
including making it more difficult for us to obtain financing on favorable terms, limiting our ability to capitalize on significant business
opportunities, and making us more vulnerable to rising interest rates.
We depend on key personnel and may not be
able to retain these employees or recruit additional qualified personnel, which could harm our business.
Our success depends to a significant extent on
the continued services of our senior management and other members of management. We have employment agreements with our CEO, CFO and division
presidents that range from one to three years. If our CEO, CFO, division presidents, or other members of senior management do not continue
in their present positions, our business may suffer. Because of the specialized scientific nature of our business, we are highly dependent
upon attracting and retaining qualified scientific and technical and managerial personnel. While we have a strong record of employee retention,
there is still significant competition for qualified personnel in the software, pharmaceutical, and biotechnology fields. Therefore, we
may not be able to attract and retain the qualified personnel necessary for the development of our business. The loss of the services
of existing personnel, as well as the failure to recruit additional key scientific, technical, and managerial personnel in a timely manner,
could harm our business.
23
If we are not successful in selecting and
integrating the businesses and technologies we acquire, or in managing our current and future divestitures, our business may suffer.
Over the years, we have expanded our business
through acquisitions. We continue to search to acquire businesses and technologies and form strategic alliances. However, businesses and
technologies may not be available on terms and conditions we find acceptable. We risk spending time and money investigating and negotiating
with potential acquisition or alliance partners, but not completing transactions. Even if completed, acquisitions and alliances involve
numerous risks which may include: difficulties in achieving business and continuing financial success; difficulties and expenses incurred
in assimilating and integrating operations, services, products, technologies, or pre-existing relationships with our customers, distributors,
and suppliers; challenges with developing and operating new businesses, including those which are materially different from our existing
businesses and which may require the development or acquisition of new internal capabilities and expertise; challenges of maintaining
staffing at the acquired entities, including loss of key employees; potential losses resulting from undiscovered liabilities of acquired
companies that are not covered by the indemnification we may obtain from the seller(s); the presence or absence of adequate internal controls
and/or significant fraud in the financial systems of acquired companies; diversion of management’s attention from other business
concerns; acquisitions could be dilutive to earnings, or in the event of acquisitions made through the issuance of our common stock to
the shareholders of the acquired company, dilutive to the percentage of ownership of our existing shareholders; new technologies and products
may be developed which cause businesses or assets we acquire to become less valuable; and risks that disagreements or disputes with prior
owners of an acquired business, technology, service, or product may result in litigation expenses and distribution of our management’s
attention. In the event that an acquired business or technology or an alliance does not meet our expectations, our results of operations
may be adversely affected.
Some of the same risks exist when we decide to
sell a business, site, or product line. In addition, divestitures could involve additional risks, including, without limitation, the following:
difficulties in the separation of operations, services, products, and personnel; and the need to agree to retain or assume certain current
or future liabilities in order to complete the divestiture. We evaluate the performance and strategic fit of our businesses. These and
any divestitures may result in significant write-offs, including those related to goodwill and other intangible assets, which could have
an adverse effect on our results of operations and financial condition. In addition, we may encounter difficulty in finding buyers or
alternative exit strategies at acceptable prices and terms and in a timely manner. We may not be successful in managing these or any other
significant risks that we encounter in divesting a business, site, or product line, and as a result, we may not achieve some or all of
the expected benefits of the divestitures.
Our quarterly and annual operating results
fluctuate and may continue to fluctuate in the future, and if we fail to meet the expectations of analysts or investors, our stock price
and the value of your investment could decline substantially .
We believe that operating results for any particular
quarter are not necessarily a meaningful indication of future results. Nonetheless, fluctuations in our quarterly operating results could
negatively affect the market price of our common stock. Our results of operations in any quarter or annual period have varied in the past
and may vary from quarter to quarter or year to year. Our results of operations are influenced by various factors, many of which are out
of our control, including without limitation:
·
changes in the general global economy;
·
the number and scope of ongoing client engagements; the commencement, postponement, delay, progress, completion, or cancellation of client contracts in the quarter;
·
changes in customer budget cycles;
·
the number and scope of ongoing client engagements;
·
the commencement, postponement, delay, progress, completion, or cancellation of client contracts in the quarter;
·
changes in the mix of our products and services;
24
·
competitive pricing pressures;
·
the extent of cost overruns;
·
buying patterns of our clients;
·
budget cycles of our clients;
·
the effect of potential acquisitions and consequent integration;
·
the timing of new product releases by us or our competitors;
·
general economic factors, including factors relating to disruptions in the world credit and equity markets and the related impact on our customers’ access to capital;
·
changes in tax laws, rules, regulations, and tax rates in the locations in which we operate;
·
the timing and charges associated with completed acquisitions and other events;
·
the financial performance of our investments; and
·
exchange rate fluctuations.
We derive a significant percentage of our
revenues from a concentrated group of customers and the loss of more than one of our major customers could materially and adversely affect
our business, results of operations or financial condition.
Three customers accounted for 11%, 4% and 3%,
respectively, of revenue for fiscal year 2021. Three customers accounted for 9%, 7% (a dealer account in Japan representing various customers),
and 7%, respectively, of revenues for fiscal year 2020. Three customers accounted for 8%, 8% and 7% (a dealer account in Japan representing
various customers), respectively, of revenues for fiscal year 2019. The loss of any of our major customers could have a material adverse
effect on our results of operations and financial condition. We may not be able to maintain our customer relationships, and our customers
may delay payment under, or fail to renew, their agreements with us, which could adversely affect our business, results of operations,
or financial condition. Any reduction in the amount of revenues that we derive from these customers, without an offsetting increase in
new revenues to other customers, could have a material adverse effect on our operating results. A significant change in the liquidity
or financial position of our customers could also have a material adverse effect on the collectability of our accounts receivable, our
liquidity, and our future operating results.
We conduct business outside the U.S., which
exposes us to foreign currency exchange rate risk, amongst other risk, and could have a negative impact on our financial results.
We operate on a global basis. In the three years
ended August 31, 2021, 2020 and 2019, we had revenues of $4.8 million, $5.0 million, and $4.1 million, respectively, denominated in foreign
currency in certain Asian and European markets. We expanded our operations in Europe in 2020 with the addition of Lixoft in Paris, France.
As we continue to increase our international operations,
our revenues and expenditures in foreign currencies are expected to become more material and subject to greater foreign currency exchange
rate fluctuations. Also, our foreign distributors typically sell our products in local currency, which impacts the price to foreign consumers.
Our subsidiary operates with their local currency as their functional currency. Future foreign currency exchange rate fluctuations and
global credit markets may cause changes in the U.S. dollar value of our purchases or sales and materially affect our revenues, profit
margins, and results of operations, when converted to U.S. dollars. Changes in the value of the U.S. dollar relative to other currencies
could result in material foreign currency exchange rate fluctuations and, as a result, our net earnings could be materially adversely
affected.
25
As we continue to expand international operations
and increase purchases and sales in foreign currencies, we may utilize derivative instruments, as needed, to hedge our foreign currency
exchange rate risk. Our hedging strategies will depend on our forecasts of revenues, expenses, and cash flows, which are inherently subject
to inaccuracies. Foreign currency exchange rate hedges, transactions, re-measurements, or translations could materially impact our consolidated
financial statements.
A significant portion of our operating expenses
is relatively fixed and planned expenditures are based in part on expectations regarding future revenues.
Accordingly, unexpected revenue shortfalls may
decrease our gross margins and could cause significant changes in our operating results from year to year. As a result, in future quarters,
our operating results could fall below the expectations of securities analysts or investors, in which event our stock price would likely
decrease.
If our customers cancel their contracts
or terminate or delay their clinical trials, we may lose or delay revenues and our business may be harmed.
Certain of our customer contracts are subject
to cancellation by our customers at any time with limited notice. Customers engaged in clinical trials may terminate or delay a clinical
trial for various reasons, including the failure of the tested product to satisfy safety or efficacy requirements, unexpected or undesired
clinical results, decisions to deemphasize a particular product or forgo a particular clinical trial, decisions to downsize clinical development
programs, insufficient patient enrollment or investigator recruitment, and production problems resulting in shortages of required clinical
supplies. Any termination or delay in the clinical trials would likely result in a consequential delay or termination in those customers’
service contracts. We have experienced terminations and delays of our customer service contracts in the past (although no such past terminations
have had a significant impact on our results of operations) and we expect to experience additional terminations and delays in the future.
The termination of single-study arrangements could result in decreased revenues and the delay of our customers’ clinical trials
could result in delayed professional services revenues, which could materially harm our business.
If our security is breached, our business
could be disrupted, our operating results could be harmed, and customers could be deterred from using our products and services.
Our business relies on the secure electronic transmission,
storage, and hosting of sensitive information, including clinical data, financial information, and other sensitive information relating
to our customers, company, and workforce. As a result, we face some risk of a deliberate or unintentional incident involving unauthorized
access to our computer systems (including, among other methods, cyber- attacks or social engineering) that could result in misappropriation
or loss of assets or sensitive information, data corruption, or other disruption of business operations. In light of this risk, we have
devoted significant resources to protecting and maintaining the confidentiality of our information, including implementing security and
privacy programs and controls, training our workforce, and implementing new technology. We have no guarantee that these programs and controls
will be adequate to prevent all possible security threats. We believe that any compromise of our electronic systems, including the unauthorized
access, use, or disclosure of sensitive information, or a significant disruption of our computing assets and networks, would adversely
affect our reputation and our ability to fulfill contractual obligations, and would require us to devote significant financial and other
resources to mitigate such problems, and could increase our future cyber security costs. Moreover, unauthorized access, use, or disclosure
of such sensitive information could result in contractual or other liability. In addition, any real or perceived compromise of our security
or disclosure of sensitive information may result in lost revenues by deterring customers from using or purchasing our products and services
in the future or prompting them to use competing service providers.
Any failure by us to properly protect customer
data we possess or are deemed to possess, in connection with the conduct of clinical trials, could subject us to significant liability.
Our customers use our solutions to collect, manage,
and report information in connection with the conduct of clinical trials. This information may be considered our customers’ proprietary
information. Since we receive and process our customers’ data from customers utilizing our hosted solutions, there is a risk that
we could be liable if there were a breach of any obligation to a protected person under contract, standard of practice, or regulatory
requirement. If we fail to properly protect our customers’ data that is in our possession or deemed to be in our possession, we
could be subjected to significant liability and our reputation would be harmed.
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We rely upon a single internal hosting facility
and Amazon Web Services to deliver certain solutions to our customers and any disruption of or interference with our hosting systems,
operations, or use of the Amazon Web Services could harm our business and results of operations.
Substantially all of the computer hardware necessary
to provide our Cognigen solutions to our customers is located at our internal hosting facility in Buffalo, New York. In addition to our
dedicated hosting facility, we utilize third-party cloud computing services from Amazon Web Services (“AWS”) to help us efficiently
scale our cloud-based solutions and provide training. Because we cannot easily switch our AWS-serviced operations to another cloud provider,
any disruption of or interference with our use of AWS would impact our operations, and our business would be adversely impacted. Our systems
and operations or those of AWS could suffer damage or interruption from human error, fire, flood, power loss, telecommunications failure,
break-ins, terrorist attacks, acts of war, and similar events. The occurrence of a natural disaster, an act of terrorism or other unanticipated
problems at our or AWS’ hosting facilities could result in lengthy interruptions in our service. Although we and AWS maintain backup
facilities and disaster recovery services in the event of a system failure, these may be insufficient or fail. Any system failure, including
network, software, or hardware failure, that causes an interruption in our Buffalo data center or our use of AWS or that causes a decrease
in responsiveness of our cloud-based solutions, could damage our reputation and cause us to lose customers, which could harm our business
and results of operations. Our business may be harmed if our customers and potential customers believe our service is unreliable.
Defects or errors in our software applications
could harm our reputation, result in significant cost to us and impair our ability to market our solutions.
Our software applications are inherently complex
and may contain defects or errors, some of which may be material. Errors may result from our own technology or from the interface of our
cloud-based solutions with legacy systems and data, which we did not develop. The risk of errors is particularly significant when a new
product is first introduced or when new versions or enhancements of existing products are released. The likelihood of errors is increased
when we do more frequent releases of new products and enhancements of existing products. We have, from time to time, found defects in
our solutions. Although these past defects have not resulted in any litigation against us to date, we have invested significant capital,
technical, managerial, and other resources to investigate and correct these past defects and we have needed to divert these resources
from other development efforts. In addition, material performance problems or defects in our solutions may arise in the future. Material
defects in our cloud-based solutions could result in a reduction in revenues, delay in market acceptance of our solutions, or credits
or refunds to our customers. In addition, such defects may lead to the loss of existing customers and difficulty in attracting new customers,
diversion of development resources, or harm to our reputation. Correction of defects or errors could prove to be impossible or impractical.
The costs incurred in correcting any defects or errors or in responding to resulting claims or liability may be substantial and could
adversely affect our operating results.
If we are not able to reliably meet our
data storage and management requirements, or if we experience any failure or interruption in the delivery of our services over the Internet,
customer satisfaction and our reputation could be harmed and customer contracts may be terminated.
As part of our current business model, we deliver
our software over the Internet and store and manage hundreds of terabytes of data for our customers, resulting in substantial information
technology infrastructure and ongoing technological challenges, which we expect to continue to increase over time. If we do not reliably
meet these data storage and management requirements, or if we experience any failure or interruption in the delivery of our services over
the Internet, customer satisfaction and our reputation could be harmed, leading to reduced revenues and increased expenses. Our hosting
services are subject to service-level agreements and, in the event that we fail to meet guaranteed service or performance levels, we could
be subject to customer credits or termination of these customer contracts. If the cost of meeting these data storage and management requirements
increases, our results of operations could be harmed.
27
Some of our software solutions and services
utilize open source software, and any failure to comply with the terms of one or more of these open source licenses could adversely affect
our business.
Some of our software solutions utilize software
covered by open-source licenses. Open-source software is typically freely accessible, usable and modifiable, and is used by our development
team in an effort to reduce development costs and speed up the development process. Certain open-source software licenses require a user
who intends to distribute the open-source software as a component of the user’s software to disclose publicly part or all of the
source code to the user’s software. In addition, certain open-source software licenses require the user of such software to make
any derivative works of the open-source code available to others on unfavorable terms or at no cost. This can subject previously proprietary
software to open-source license terms. While we monitor the use of all open-source software in our products, processes, and technology
and try to ensure that no open-source software is used in such a way as to require us to disclose or make available the source code to
the related product or solution, such use could inadvertently occur. This could harm our intellectual property position and have a material
adverse effect on our business.
We may be unable to adequately enforce or
defend our ownership and use of our intellectual property and other proprietary rights .
Our success is heavily dependent upon our intellectual
property and other proprietary rights. We rely upon a combination of trademark, trade secret, copyright, patent, and unfair competition
laws, as well as license and access agreements and other contractual provisions, to protect our intellectual property and other proprietary
rights. In addition, we attempt to protect our intellectual property and proprietary information by requiring certain of our employees
and consultants to enter into confidentiality, noncompetition, and assignment-of-inventions agreements. The steps we take to protect our
intellectual property rights may not be adequate to prevent misappropriation of our technology by third parties, or may not be adequate
under the laws of some foreign countries, which may not protect our intellectual property rights to the same extent as do the laws of
the United States.
The laws of some foreign countries do not protect
intellectual property rights to the same extent as the laws of the United States. Many companies have encountered significant problems
in protecting and defending intellectual property rights in certain foreign jurisdictions. This could make it difficult for us to stop
infringement or the misappropriation of our intellectual property rights.
Our attempts to protect our intellectual property
may be challenged by others or invalidated through administrative process or litigation, and agreement terms that address noncompetition
are difficult to enforce in many jurisdictions and may not be enforceable in any particular case. In addition, there remains the possibility
that others will “reverse engineer” our products in order to introduce competing products, or that others will develop competing
technology independently. If we resort to legal proceedings to enforce our intellectual property rights or to determine the validity and
scope of the intellectual property or other proprietary rights of others, the proceedings could be burdensome and expensive, even if we
were to prevail. The failure to adequately protect our intellectual property and other proprietary rights may have a material adverse
effect on our business, results of operations or financial condition.
Current and future litigation against us,
which may arise in the ordinary course of our business, could be costly and time-consuming to defend.
We are subject to claims that arise in the ordinary
course of business, such as claims brought by our customers in connection with commercial disputes and employment claims made by our current
or former employees. Third parties may in the future assert intellectual property rights to technologies that are important to our business
and demand back royalties or demand that we license their technology. Litigation may result in substantial costs and may divert management’s
attention and resources, which may seriously harm our business, overall financial condition, and operating results. Insurance may not
cover such claims, may not be sufficient for one or more such claims, and may not continue to be available on terms acceptable to us.
A claim brought against us that is uninsured or underinsured could result in unanticipated costs, negatively affecting our business, results
of operations, and financial condition.
28
We could incur substantial costs resulting
from product liability claims relating to our products or services or our customers’ use of our products or services.
Any failure or errors in a customer’s clinical
trial caused or allegedly caused by our products or services could result in a claim for substantial damages against us by our customers
or the clinical trial participants, regardless of our responsibility for the failure. Although we are generally entitled to indemnification
under our customer contracts against claims brought against us by third parties arising out of our customers’ use of our products,
we might find ourselves entangled in lawsuits against us that, even if unsuccessful, may divert our resources and energy and adversely
affect our business. Further, in the event we seek indemnification from a customer, a court may not enforce our indemnification right
if the customer challenges it or the customer may not be able to fund any amounts for indemnification owed to us. In addition, our existing
insurance coverage may not continue to be available on reasonable terms or may not be available in amounts sufficient to cover one or
more large claims, or the insurer may disclaim coverage as to any future claim.
Our business depends on the clinical trial
market, and a downturn in this market could cause our revenues to decrease.
Our business depends on clinical trials conducted
or sponsored by pharmaceutical, biotechnology, and medical device companies, CROs, and other entities. Our revenues may decline as a result
of conditions affecting these industries, including general economic downturns, increased consolidation, decreased competition, or fewer
products under development. Other developments that may affect these industries and harm our operating results include product liability
claims, changes in government regulation, changes in governmental price controls or third-party reimbursement practices, and changes in
medical practices. Disruptions in the world credit and equity markets may also result in a global downturn in spending on research and
development and clinical trials and may impact our customers’ access to capital and their ability to pay for our solutions. Any
decrease in research and development expenditures or in the size, scope, or frequency of clinical trials could materially adversely affect
our business, results of operations, or financial condition.
As a public company, we are obligated to
maintain proper and effective internal control over financial reporting. As our business expands both organically and through acquisitions,
we may be unable to effectively adapt our current systems to our changing business needs and may fail to develop and maintain an effective
system of disclosure controls and internal control over financial reporting which could impair our ability to produce timely and accurate
financial statements or comply with applicable laws and regulations.
As a public company, we are subject to the reporting
requirements of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), the Sarbanes-Oxley Act of 2002 (the
“Sarbanes-Oxley Act”), the Dodd-Frank Wall Street Reform and Consumer Protection Act of 2010 (the “Dodd-Frank Act”),
and other applicable securities rules and regulations. Compliance with these rules and regulations will increase our legal and financial
compliance costs, make some activities more difficult, time consuming, or costly, and increase demand on our systems and resources. The
Exchange Act requires, among other things, that we file annual, quarterly, and current reports with respect to our business and operating
results. The Sarbanes-Oxley Act requires, among other things, that we maintain effective disclosure controls and procedures and internal
control over financial reporting. As a company, we continually review and evaluate the adequacy of our disclosure controls and procedures
and internal controls over financial reporting for deficiencies and improvements.
As we expand our operations through acquisitions
and organic growth, our current systems for disclosure controls and procedures and internal control over financial reporting may be inadequate
to meet our growing and changing business. Accordingly, we may require significant resources and management oversight to maintain and,
if necessary, improve our disclosure controls and procedures and internal control over financial reporting. As a result, management’s
attention may be diverted from other business concerns, which could adversely affect our business and operating results. In addition,
we may need to hire more employees in the future or engage outside consultants with respect to developing and maintaining our disclosure
controls and internal control over financial reporting, which would increase our costs and expenses.
29
In addition, as a public company, we are required,
pursuant to Section 404 of the Sarbanes-Oxley Act to furnish a report by management on, among other things, the effectiveness of
our internal control over financial reporting. Effective internal control over financial reporting is necessary for us to provide reliable
financial reports and, together with adequate disclosure controls and procedures, are designed to prevent fraud. As a result of
the growth of our business both organically and through acquisitions, we may fail to implement required new or improved controls, or experience
difficulties in their implementation, which may cause us to not meet our reporting obligations. If we or our independent registered public
accounting firm were to identify a material weakness, if we are unable to assert that our internal control over financial reporting is
effective, we could lose investor confidence in the accuracy and completeness of our financial reports, which could cause the price of
our common stock to decline, and we may be subject to investigation by the SEC.
As a public company, we may incur significant
administrative workload and expenses in connection with new and changing compliance requirements .
As a public company with common stock listed on
The Nasdaq Global Select Market, we must comply with various laws, regulations and requirements. New laws and regulations, as well as
changes to existing laws and regulations affecting public companies, including the provisions of the Sarbanes-Oxley Act, the Dodd-Frank
Act, and rules adopted by the SEC and by the Nasdaq Global Select Market, may result in increased general and administrative expenses
and a diversion of management’s time and attention as we respond to new requirements.
Certain Risks Related to Ownership of Our Common
Stock
We have been paying quarterly dividends
on shares of our common stock, and although there has been a consistent track record of paying these dividends, the Board of Directors
may suspend the dividend, and, consequently, your ability to achieve a return on your investment will depend on appreciation in the price
of our common stock.
Should the Board of Directors suspend the dividend
and decide to use those funds to invest more into our business, you may not receive any dividends on your investment in our common stock
for the foreseeable future and the success of an investment in shares of our common stock will depend upon any future appreciation in
its value. Shares of our common stock may depreciate in value or may not appreciate in value.
If our operating and financial performance
in any given period does not meet any guidance that we provide to the public, the market price of our common stock may decline.
We may, but are not obligated to, provide public
guidance on our expected operating and financial results for future periods. Any such guidance will be comprised of forward-looking statements
subject to the risks and uncertainties described in this prospectus and in our other public filings and public statements. Our actual
results may not always be in line with or exceed any guidance we have provided, especially in times of economic uncertainty. If, in the
future, our operating or financial results for a particular period do not meet any guidance we provide or the expectations of investment
analysts, or if we reduce our guidance for future periods, the market price of our common stock may decline. Even if we do issue public
guidance, there can be no assurance that we will continue to do so in the future.
30
The price of our common stock may fluctuate
significantly, and investors could lose all or part of their investments.
Shares of our common stock were sold in our initial
public offering (“IPO”) in 1996 at a price of $1.25 per share (on a post-split basis), and our common stock has subsequently
traded as high as $90.92 and as low as $0.38 from our IPO through August 31, 2021. However, an active, liquid, and orderly market for
our common stock on the Nasdaq Global Select Market or otherwise may not be sustained, which could depress the trading price of our common
stock. The trading price of our common stock may be subject to wide fluctuations in response to various factors, some of which are beyond
our control, including without limitation:
·
our quarterly or annual earnings or those of other companies in our industry;
·
announcements by us or our competitors of significant contracts or acquisitions;
·
changes in accounting standards, policies, guidance, interpretations, or principles;
·
general economic and stock market conditions, including disruptions in the world credit and equity markets;
·
the failure of securities analysts to cover our common stock or changes in financial estimates by analysts;
·
future sales of our common stock; and
·
the other factors described in these “Risk Factors.”
In recent years, the stock market in general,
and the market for technology-related companies in particular, has experienced wide price and volume fluctuations. This volatility has
had a significant impact on the market price of securities issued by many companies, including companies in our industry. The price of
our common stock could fluctuate based upon factors that have little to do with our performance, and these fluctuations could materially
reduce our stock price.
In the past, some companies, including companies
in our industry, have had volatile market prices for their securities and have had securities class action suits filed against them.
The filing of a lawsuit against us, regardless of the outcome, could have a material adverse effect on our business, financial condition,
and results of operations, as it could result in substantial legal costs and a diversion of our management’s attention and resources.
The price of our common stock may be volatile,
and our stockholders may not be able to resell shares of our common stock at or above the price they paid.
The trading price of our common stock is volatile
and could be subject to wide fluctuations in response to various factors, some of which are beyond our control. Factors that could cause
volatility in the market price of our common stock include, but are not limited to:
·
achievement of expected software product and consulting service revenues and profitability, including the effects of seasonality on our results of operations, as well as adjustments to our revenues forecasts;
·
the ongoing COVID-19 pandemic, see “—Certain Risks Related to our Business—Our business is subject to risks arising from epidemic diseases, such as the recent outbreak of the COVID-19 illness.”
·
announcements of new products by us or our competitors;
·
announcements or developments in any intellectual property infringement actions in which we may become involved;
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·
our operating results;
·
results from, or any delays in, clinical trial programs of our clients and their need for our services;
·
changes or developments in laws or regulations applicable to our products;
·
consolidation within the pharmaceutical and
biotechnology industries leading to fewer potential customers for our products and services;
·
delays in the release of new or enhanced products or services or undetected errors in our products or services may result in increased cost to us, delayed market acceptance of our products, and delayed or lost revenue;
·
adverse actions taken by regulatory agencies with respect to our clinical trials, manufacturing supply chain, or sales and marketing activities;
·
the success of our efforts to acquire or develop additional products;
·
announcements concerning our competitors or the pharmaceutical industry in general;
·
actual or anticipated fluctuations in our operating results;
·
FDA or other U.S. or foreign regulatory actions affecting us or our industry or other healthcare reform measures in the United States;
·
changes in financial estimates or recommendations by securities analysts;
·
trading volume of our common stock;
·
sales of our common stock by us, our executive officers and directors, or our stockholders in the future;
·
general economic and market conditions and overall fluctuations in the United States equity markets, including as a result of volatility related to the recent coronavirus outbreak and related health concerns; and
·
the loss of any of our key scientific or management personnel.
Broad market fluctuations may adversely affect
the trading price or liquidity of our common stock. In the past, when the market price of a stock has been volatile, holders of that stock
have sometimes instituted securities class action litigation against the issuer. If any of our stockholders were to bring such a lawsuit
against us, we could incur substantial costs defending the lawsuit and the attention of our management would be diverted from the operation
of our business, which could seriously harm our financial position. Any adverse determination in litigation could also subject us to significant
liabilities.
If securities or industry analysts issue
an adverse or misleading opinion regarding our stock, or our inclusion in the S&P 600 discontinues, our stock price and trading volume
could decline.
The trading market for our common stock is influenced
by the research and reports that industry or securities analysts publish about us or our business as well as the stock indices that our
common stock is included in. If any of the analysts who cover us issue an adverse or misleading opinion regarding us, our business model,
our intellectual property or our stock performance, or if our operating results fail to meet the expectations of analysts, our stock price
would likely decline. If one or more of these analysts cease coverage of us or fail to publish reports on us regularly, or if the S&P
600 removes us from its index, we could lose visibility in the financial markets, which in turn could cause our stock price or trading
volume to decline.
32
We may raise capital through the issuance
of our common stock, convertible debt or equity linked securities, which could result in dilution to our stockholders or negatively impact
the price of our common stock.
In August 2020 we issued 2,090,909 shares of our
common stock in a follow-on public offering. We may choose to raise additional capital due to market conditions or strategic considerations.
To the extent that additional capital is raised through the sale of equity, convertible debt or other equity linked securities, the issuance
of these securities could result in dilution to our stockholders or result in downward pressure on the price of our common stock.
ITEM 1B – UNRESOLVED STAFF COMMENTS
None.
Text extracted from the filing as submitted to EDGAR. Formatting, tables and exhibits are simplified for reading; the original document is authoritative for anything you rely on.