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Additional risks and uncertainties of which we are not presently aware, or that we currently consider immaterial, may also impair our business operations.
−Removed: The risk factors set forth below that are marked with an asterisk (*) contain changes to the similarly titled risk factors included in Part I, Item 1A of our Annual Report.
+Added: Summary of Risk Factors
+Added: We are providing the following summary of the risk factors contained in our Form 10-Q to enhance the readability and accessibility of our risk factor disclosures.
+Added: We encourage our stockholders to carefully review the risk factors contained in this Form 10-Q in their entirety for additional information regarding the risks and uncertainties that could cause our actual results to vary materially from recent results or from our anticipated future results.
+Added: ▪ The COVID-19 pandemic has adversely affected, and is expected to continue to pose risks to, our business, results of operations, financial condition and cash flows, and other epidemics or outbreaks of infectious diseases may have a similar impact.
+Added: ▪ Global, market and economic conditions may negatively impact our business, financial condition and share price.
+Added: ▪ We have a history of operating losses, may need additional financing to meet our future long-term capital requirements and may be unable to raise sufficient capital on favorable terms or at all.
+Added: ▪ Interruptions in our relationships or declines in our business with major customers could materially harm our business and financial results.
+Added: ▪ Our future success largely depends on sales of our Tru Niagen® product.
+Added: ▪ The success of our consumer product and ingredient business is linked to the size and growth rate of the vitamin, mineral and dietary supplement market and an adverse change in the size or growth rate of that market could have a material adverse effect on us.
+Added: ▪ The future growth and profitability of our consumer product business will depend in large part upon the effectiveness and efficiency of our marketing efforts and our ability to select effective markets and media in which to market and advertise.
+Added: ▪ Many of our competitors are larger and have greater financial and other resources than we do.
+Added: ▪ Our operating results may fluctuate significantly as a result of a variety of factors, many of which are outside of our control.
+Added: ▪ If we are unable to maintain sales, marketing and distribution capabilities or maintain arrangements with third parties to sell, market and distribute our products, our business may be harmed.
+Added: ▪ Our failure to establish and maintain effective internal control over financial reporting could result in material misstatements in our financial statements, result in our failure to meet our reporting obligations and cause investors to lose confidence in our reported financial information, which in turn could cause the trading price of our common stock to decline.
+Added: ▪ Our business could be negatively impacted by cyber security incidents or threats, including without limitation a material interruption to our operations including our clinical trials, harm to our reputation, significant fines, penalties and liabilities, regulatory investigations or actions, breach or triggering of data protection laws, privacy policies and data protection obligations, or a loss of revenue, customers or sales.
+Added: ▪ Unfavorable publicity or consumer perception of our products and any similar products distributed by other companies could have a material adverse effect on our business.
+Added: ▪ We may incur material product liability claims, which could increase our costs and adversely affect our reputation, revenues and operating income.
+Added: ▪ We utilize ingredients and components for our products from foreign suppliers, and may be negatively affected by the risks associated with international trade and importation issues.
+Added: ▪ We rely on single or a limited number of third-party suppliers for the raw materials required to produce our products.
+Added: ▪ Our ability to protect our intellectual property and proprietary technology through patents and other means is uncertain and may be inadequate, which would have a material and adverse effect on us.
+Added: ▪ Our patents and licenses may be subject to challenge on validity grounds, and our patent applications may be rejected.
+Added: ▪ We may become subject to claims of infringement or misappropriation of the intellectual property rights of others, which could prohibit us from developing our products, require us to obtain licenses from third parties or to develop non-infringing alternatives and subject us to substantial monetary damages.
+Added: ▪ We are currently engaged in substantial and complex litigation with Elysium Health, Inc.
+Added: and Elysium Health LLC (collectively, “Elysium”), the outcome of which could materially harm our business and financial results.
+Added: ▪ Changes in government regulation or in practices relating to the pharmaceutical, dietary supplement, food and cosmetic industry could decrease the need for the services we provide.
+Added: ▪ Compliance with stringent and changing global privacy and data security laws and regulations could result in additional costs and liabilities to us or inhibit our ability to collect and, if applicable, process data globally, and the failure or perceived failure to comply with such laws and regulations could have a material adverse effect on our business, financial condition or results of operations.
+Added: ▪ The market price of our common stock may be volatile and adversely affected by several factors.
+Added: ▪ We have not paid cash dividends in the past and do not expect to pay cash dividends in the foreseeable future.
+Added: Any return on investment may be limited to the value of our common stock.
+Added: ▪ We have a significant number of outstanding options and unvested restricted stock units.
+Added: Future sales of these shares could adversely affect the market price of our common stock.
+Added: ▪ We may become involved in securities class action litigation that could divert management’s attention and harm our business.
Risks Related to our Company and our Business
The COVID-19 pandemic has adversely affected, and is expected to continue to pose risks to, our business, results of operations, financial condition and cash flows, and other epidemics or outbreaks of infectious diseases may have a similar impact.
−Removed: As previously disclosed, we face risks related to the ongoing COVID-19 pandemic, including the emergence of new variant strains and these variant strains impacts.
+Added: As previously disclosed, we face risks related to the ongoing COVID-19 pandemic, including the emergence of new variant strains with varying degrees of resistance to vaccines, and these variant strains’ impacts.
COVID-19 has spread across the globe since 2020 and is impacting economic activity worldwide.
−Removed: COVID-19 has caused disruption and volatility in the global capital markets, and has caused an economic slowdown.
+Added: COVID-19 has caused supply chain and market disruptions and volatility in the global capital markets, and has caused an economic slowdown.
In response to COVID-19, national and local governments around the world have instituted certain measures, including travel bans, prohibitions on group events and gatherings, shutdowns of certain businesses, curfews, shelter-in-place orders, vaccine mandates and recommendations to practice social distancing.
−Removed: The duration of these measures is unknown, may be extended and additional measures may be imposed, which could negatively impact our sales volumes.
+Added: The duration of these measures is unknown, may be extended and additional measures may be imposed, in light of the recent surge in cases, which could negatively impact our sales volumes.
The potential effects of COVID-19 include, but are not limited to, the following:
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• Reduced demand for our products due to store closures and reduced operating hours of our customers.
−Removed: • Disruptions in supply chain, leading to inadequate levels of inventory that may lower our sales.
+Added: • Disruptions in supply chain, leading to inadequate levels of inventory that may lower our sales and/or rising inflationary pressures that may increase our cost of goods.
For example, our retail business, including sales to A.S.
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The ultimate impact of COVID-19 on our business, results of operations, financial condition and cash flows is dependent on future developments, including the duration of the pandemic and the related length of its impact on the global economy, which are uncertain and cannot be predicted at this time.
+Added: Global, market and economic conditions may negatively impact our business, financial condition and share price.
+Added: Concerns over inflation, geopolitical issues, the U.S.
+Added: financial markets, foreign exchange rates, capital and exchange controls, unstable global credit markets and financial conditions and the COVID-19 pandemic, have led to periods of significant economic instability, declines in consumer confidence and discretionary spending, diminished expectations for the global economy and expectations of slower global economic growth going forward, and increased unemployment rates.
+Added: Our general business strategy may be adversely affected by any such economic downturns, volatile business environments and continued unstable or unpredictable economic and market conditions.
+Added: If these conditions continue to deteriorate or do not improve, it may make any necessary debt or equity financing more difficult to complete, more costly and more dilutive.
+Added: In addition, there is a risk that one or more of our current or future service providers, manufacturers, suppliers and other partners could be negatively affected by difficult economic times, which could adversely affect our ability to attain our operating goals on schedule and on budget or meet our business and financial objectives.
+Added: In addition, we face several risks associated with international business and are subject to global events beyond our control, including war, public health crises, such as pandemics and epidemics, trade disputes, economic sanctions, trade wars and their collateral impacts and other international events.
+Added: Any of these changes could have a material adverse effect on our reputation, business, financial condition or results of operations.
+Added: There may be changes to our business if there is instability, disruption or destruction in a significant geographic region, regardless of cause, including war, terrorism, riot, civil insurrection or social unrest;
+Added: and natural or man-made disasters, including famine, flood, fire, earthquake, storm or disease.
+Added: In February 2022, armed conflict escalated between Russia and Ukraine.
+Added: The sanctions announced by the U.S.
+Added: and other countries, following Russia’s invasion of Ukraine against Russia to date include restrictions on selling or importing goods, services or technology in or from affected regions and travel bans and asset freezes impacting connected individuals and political, military, business and financial organizations in Russia.
+Added: and other countries could impose wider sanctions and take other actions should the conflict further escalate.
+Added: It is not possible to predict the broader consequences of this conflict, which could include further sanctions, embargoes, regional instability, geopolitical shifts and adverse effects on macroeconomic conditions, currency exchange rates and financial markets, all of which could impact our business, financial condition and results of operations.
We have a history of operating losses, may need additional financing to meet our future long-term capital requirements and may be unable to raise sufficient capital on favorable terms or at all.
−Removed: We have recorded a net loss of approximately $21.8 million for the nine months ended September 30, 2021 and we have a history of losses and may continue to incur operating and net losses for the foreseeable future.
+Added: We have recorded a net loss of approximately $7.7 million for the three months ended March 31, 2022 and we have a history of losses and may continue to incur operating and net losses for the foreseeable future.
We incurred net losses of approximately $27.1 million and $19.9 million for the years ended December 31, 2021 and December 31, 2020, respectively.
−Removed: As of September 30, 2021, our accumulated deficit was approximately $163.6 million.
+Added: As of March 31, 2022, our accumulated deficit was approximately $176.7 million.
We have not achieved profitability on an annual basis.
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If our revenues grow slower than anticipated, or if operating expenses exceed expectations, then we may not be able to achieve and sustain profitability in the near future or at all, which may depress our stock price.
−Removed: As of September 30, 2021, our cash and cash equivalents totaled approximately $33.1 million.
−Removed: While we anticipate that our current cash, cash equivalents, cash to be generated from operations and available line of credit up to $7.0 million from Western Alliance Bank will be sufficient to meet our projected operating plans through at least the next twelve months, we may require additional funds, either through additional equity or debt financings, including pursuant to the At Market Issuance Sales Agreement, dated as of June 12, 2020, with B.
+Added: As of March 31, 2022, our cash and cash equivalents totaled approximately $21.0 million and we had no borrowings outstanding under our line of credit up to $10.0 million with Western Alliance Bank.
+Added: While we anticipate that our current cash, cash equivalents and cash to be generated from net sales will be sufficient to meet our projected operating plans through at least the next twelve months, we may require additional funds, either through additional equity or debt financings, including pursuant to the At Market Issuance Sales Agreement, dated as of June 12, 2020, with B.
Riley FBR, Inc.
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(ATM Facility), or collaborative agreements or from other sources.
−Removed: Our line of credit currently expires on November 12, 2021.
−Removed: We are actively working with Western Alliance Bank to extend this line of credit prior to its expiration.
−Removed: The line of credit is an additional source of liquidity available to us, however any inability to access any portion of the amount available under this line will not have an adverse effect on our ability to satisfy our obligations or support operations.
−Removed: We do not believe any delays in or inability to obtain an extension of this line of credit will impact our ability to meet our operating objectives for at least the next twelve months.
We have no commitments to obtain such additional financing, and we may not be able to obtain any such additional financing on terms favorable to us, or at all.
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The inability to raise additional financing may have a material adverse effect on the future performance of the Company.
−Removed: Our capital requirements will depend on many factors.
−Removed: Our capital requirements will depend on many factors, including:
+Added: Our material cash requirements will depend on many factors.
+Added: Our material cash requirements will depend on many factors, including:
• the revenues generated by sales of our products;
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• the expenses we incur in developing and commercializing our products, including the cost of obtaining and maintaining regulatory approvals;
−Removed: • unanticipated general and administrative expenses, including expenses involved with our ongoing litigation.
+Added: • unanticipated general and administrative expenses.
Because of these factors, we may seek to raise additional capital within the next twelve months both to meet our projected operating plans after the next twelve months and to fund our longer term strategic objectives.
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Any of these events could adversely affect our ability to achieve our development and commercialization goals, which could have a material and adverse effect on our business, results of operations and financial condition.
−Removed: Our ability to protect our intellectual property and proprietary technology through patents and other means is uncertain and may be inadequate, which would have a material and adverse effect on us.
−Removed: Our success depends significantly on our ability to protect our proprietary rights to the technologies used in our products.
−Removed: We rely on patent protection, as well as a combination of copyright, trade secret and trademark laws and nondisclosure, confidentiality and other contractual restrictions to protect our proprietary technology, including our licensed technology.
−Removed: However, these legal means afford only limited protection and may not adequately protect our rights or permit us to gain or keep any competitive advantage.
−Removed: For example, our pending United States and foreign patent applications may not issue as patents in a form that will be advantageous to us or may issue and be subsequently successfully challenged by others and invalidated.
−Removed: In addition, our pending patent applications include claims to material aspects of our products and procedures that are not currently protected by issued patents.
−Removed: Both the patent application process and the process of managing patent disputes can be time consuming and expensive.
−Removed: Competitors may be able to design around our patents or develop products which provide outcomes which are comparable or even superior to ours.
−Removed: Steps that we have taken to protect our intellectual property and proprietary technology, including entering into confidentiality agreements and intellectual property assignment agreements with some of our officers, employees, consultants and advisors, may not provide us with meaningful protection for our trade secrets or other proprietary information in the event of unauthorized use or disclosure or other breaches of the agreements.
−Removed: Furthermore, the laws of foreign countries may not protect our intellectual property rights to the same extent as do the laws of the United States.
−Removed: In the event a competitor infringes our licensed or pending patent or other intellectual property rights, enforcing those rights may be costly, uncertain, difficult and time consuming.
−Removed: Even if successful, litigation to enforce our intellectual property rights or to defend our patents against challenge could be expensive and time consuming and could divert our management’s attention.
−Removed: We may not have sufficient resources to enforce our intellectual property rights or to defend our patents rights against a challenge.
−Removed: The failure to obtain patents and/or protect our intellectual property rights could have a material and adverse effect on our business, results of operations and financial condition.
−Removed: *Our patents and licenses may be subject to challenge on validity grounds, and our patent applications may be rejected.
−Removed: We rely on our patents, patent applications, licenses and other intellectual property rights to give us a competitive advantage.
−Removed: Whether a patent is valid, or whether a patent application should be granted, is a complex matter of science and law, and therefore we cannot be certain that, if challenged, our patents, patent applications and/or other intellectual property rights would be upheld nor can we be certain we will prevail in an appeal.
−Removed: If one or more of those patents, patent applications, licenses and other intellectual property rights are invalidated, rejected or found unenforceable and we are unable to reverse that finding through an appeal, that could reduce or eliminate any competitive advantage we might otherwise have had.
−Removed: We may become subject to claims of infringement or misappropriation of the intellectual property rights of others, which could prohibit us from developing our products, require us to obtain licenses from third parties or to develop non-infringing alternatives and subject us to substantial monetary damages.
−Removed: Third parties could, in the future, assert infringement or misappropriation claims against us with respect to products we develop.
−Removed: Whether a product infringes a patent or misappropriates other intellectual property involves complex legal and factual issues, the determination of which is often uncertain.
−Removed: Therefore, we cannot be certain that we have not infringed the intellectual property rights of others.
−Removed: There may be third-party patents or patent applications with claims to materials, formulations, methods of manufacture or methods for use related to the use or manufacture of our products, and our potential competitors may assert that some aspect of our product infringes their patents.
−Removed: Because patent applications may take years to issue, there also may be applications now pending of which we are unaware that may later result in issued patents upon which our products could infringe.
−Removed: There also may be existing patents or pending patent applications of which we are unaware upon which our products may inadvertently infringe.
−Removed: Any infringement or misappropriation claim could cause us to incur significant costs, place significant strain on our financial resources, divert management’s attention from our business and harm our reputation.
−Removed: If the relevant patents in such claim were upheld as valid and enforceable and we were found to infringe them, we could be prohibited from manufacturing or selling any product that is found to infringe unless we could obtain licenses to use the technology covered by the patent or are able to design around the patent.
−Removed: We may be unable to obtain such a license on terms acceptable to us, if at all, and we may not be able to redesign our products to avoid infringement, which could materially impact our revenue.
−Removed: A court could also order us to pay compensatory damages for such infringement, plus prejudgment interest and could, in addition, treble the compensatory damages and award attorney fees.
−Removed: These damages could be substantial and could harm our reputation, business, financial condition and operating results.
−Removed: A court also could enter orders that temporarily, preliminarily or permanently enjoin us and our customers from making, using, or selling products, and could enter an order mandating that we undertake certain remedial
−Removed: Depending on the nature of the relief ordered by the court, we could become liable for additional damages to third parties.
−Removed: The prosecution and enforcement of patents licensed to us by third parties are not within our control.
−Removed: Without these technologies, our products may not be successful and our business would be harmed if the patents were infringed on or misappropriated without action by such third parties.
−Removed: We have obtained licenses from third parties for patents and patent application rights related to ingredients and/or the products we are developing, allowing us to use intellectual property rights owned by or licensed to these third parties.
−Removed: We do not control the maintenance, prosecution, enforcement or strategy for many of these patents or patent application rights and as such are dependent in part on the owners of the intellectual property rights to maintain their viability.
−Removed: If any third-party licensor is unable to successfully maintain, prosecute or enforce the licensed patents and/or patent application rights related to our products, we may become subject to infringement or misappropriate claims or lose our competitive advantage.
−Removed: Without access to these technologies or suitable design-around or alternative technology options, our ability to conduct our business could be impaired significantly.
−Removed: *We are currently engaged in substantial and complex litigation with Elysium Health, Inc.
−Removed: and Elysium Health LLC (collectively, "Elysium"), the outcome of which could materially harm our business and financial results.
−Removed: The litigation includes multiple complaints and counterclaims by us and Elysium in venues in California and New York, as well as a patent infringement complaint filed by the Company and Trustees of Dartmouth College.
−Removed: For further details on this litigation, please refer to Note 12, Commitments and Contingencies, Legal Proceedings in the Notes to the Consolidated Financial Statements, included in Part I, Item 1 of this Quarterly Report on Form 10-Q.
−Removed: The litigation is substantial and complex, and it has caused and could continue to cause us to incur significant costs, as well as distract our management over an extended period.
−Removed: The litigation may substantially disrupt our business and we cannot assure you that we will be able to resolve the litigation on terms favorable to us.
−Removed: If we are unsuccessful in resolving the litigation on favorable terms to us, we may be forced to pay compensatory and punitive damages and restitution for any royalty payments that we received from Elysium, which payments could materially harm our business, or be subject to other remedies, including injunctive relief.
−Removed: We cannot predict the outcome of our litigation with Elysium, which could have any of the results described above or other results that could materially adversely affect our business.
Interruptions in our relationships or declines in our business with major customers could materially harm our business and financial results.
−Removed: Watson Group accounted for approximately 14% of our sales during the nine months ended September 30, 2021.
+Added: Watson Group accounted for approximately 14.8% of our sales during the three months ended March 31, 2022.
Any interruption in our relationship or decline in our business with this customer or other customers upon whom we become highly dependent could cause harm to our business.
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As a result, the market acceptance of Tru Niagen® is critical to our continued success, and if we are unable to expand market acceptance of Tru Niagen®, our business, results of operations, financial condition, liquidity and growth prospects would be materially adversely affected.
−Removed: Our TRU NIAGEN ® products are not approved by the United States Food and Drug Administration or any foreign regulatory authority to mitigate, prevent, treat, diagnose or cure COVID-19 or any other disease or condition.
−Removed: In November 2020, we received a warning letter (the Letter) from the FDA and Federal Trade Commission (FTC) and in April 2021 we received an additional warning letter from only the FTC (the Second Letter).
−Removed: For more information, see Note 12, Commitments and Contingencies, Contingencies in the Notes to the Consolidated Financial Statements, included in Part I, Item 1 of this Quarterly Report on Form 10-Q.
−Removed: Our TRU NIAGEN® products are not approved by the FDA or any foreign regulatory authority to mitigate, prevent, treat, diagnose or cure COVID-19 or any other disease or condition, and are not intended for such use, and may never be approved for such use by the FDA or any foreign regulatory authority.
−Removed: We have completed and ongoing COVID-19 research on nicotinamide riboside (NR), including NR in combination with other ingredients.
−Removed: We cannot guarantee that these studies will be completed and, if so, that they will show a benefit of NR on COVID-19 patients.
−Removed: Furthermore, we cannot guarantee that the nutritional protocol including NR will be approved by the Ministry of Health in Turkey, or that these scientific studies will otherwise translate into future revenues for ChromaDex.
Decline in the state of the global economy and financial market conditions could adversely affect our ability to conduct business and our results of operations .
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Such events could, in turn, adversely affect our business through loss of sales.
−Removed: We may need to increase the size of our organization, and we can provide no assurance that we will successfully expand operations or manage growth effectively.
−Removed: Our significant increase in the scope and the scale of our product launches, including the hiring of additional personnel, has resulted in significantly higher operating expenses.
−Removed: As a result, we anticipate that our operating expenses will continue to increase.
−Removed: Expansion of our operations may also cause a significant demand on our management, finances and other resources.
−Removed: Our ability to manage the anticipated future growth, should it occur, will depend upon a significant expansion of our accounting and other internal management systems and the implementation and subsequent improvement of a variety of systems, procedures and controls.
−Removed: There can be no assurance that significant problems in these areas will not occur.
−Removed: Any failure to expand these areas and implement and improve such systems, procedures and controls in an efficient manner at a pace consistent with our business could have a material adverse effect on our business, financial condition and results of operations.
−Removed: There can be no assurance that our attempts to expand our marketing, sales, manufacturing and customer support efforts will be successful or will result in additional sales or profitability in any future period.
−Removed: As a result of the expansion of our operations and the anticipated increase in our operating expenses, as well as the difficulty in forecasting revenue levels, we expect to continue to experience significant fluctuations in our results of operations.
Changes in our business strategy, including entering the consumer product market, or restructuring of our businesses may increase our costs or otherwise affect the profitability of our businesses.
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In any of these events, our costs may increase, we may have significant charges associated with the write-down of assets or returns on new investments may be lower than prior to the change in strategy or restructuring.
−Removed: For example, if we are not successful in developing our consumer product business, our sales may decrease and our costs may increase.
+Added: For example, we may not be successful in developing our consumer product business for sales of Tru Niagen® products, and our sales may decrease despite us incurring increased costs related to marketing such products.
The success of our consumer product and ingredient business is linked to the size and growth rate of the vitamin, mineral and dietary supplement market and an adverse change in the size or growth rate of that market could have a material adverse effect on us.
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• convert consumer inquiries into actual orders.
−Removed: Unfavorable publicity or consumer perception of our products and any similar products distributed by other companies could have a material adverse effect on our business.
−Removed: We believe the nutritional supplement market is highly dependent upon consumer perception regarding the safety, efficacy and quality of nutritional supplements generally, as well as of products distributed specifically by us.
−Removed: Consumer perception of our products can be significantly influenced by scientific research or findings, regulatory investigations, litigation, national media attention and other publicity regarding the consumption of nutritional supplements.
−Removed: We cannot assure you that future scientific research, findings, regulatory proceedings, litigation, media attention or other favorable research findings or publicity will be favorable to the nutritional supplement market or any product, or consistent with earlier publicity.
−Removed: Future research reports, findings, regulatory proceedings, litigation, media attention or other publicity that are perceived as less favorable than, or that question, such earlier research reports, findings or publicity could have a material adverse effect on the demand for our products and consequently on our business, results of operations, financial condition and cash flows.
−Removed: Our dependence upon consumer perceptions means that adverse scientific research reports, findings, regulatory proceedings, litigation, media attention or other publicity, if accurate or with merit, could have a material adverse effect on the demand for our products, the availability and pricing of our ingredients, and our business, results of operations, financial condition and cash flows.
−Removed: Further, adverse public reports or other media attention regarding the safety, efficacy and quality of nutritional supplements in general, or our products specifically, or associating the consumption of nutritional supplements with illness, could have such a material adverse effect.
−Removed: Any such adverse public reports or other media attention could arise even if the adverse effects associated with such products resulted from consumers’ failure to consume such products appropriately or as directed and the content of such public reports and other media attention may be beyond our control.
−Removed: We may incur material product liability claims, which could increase our costs and adversely affect our reputation, revenues and operating income .
−Removed: As a consumer product and ingredient supplier we market and manufacture products designed for human and animal consumption.
−Removed: We are subject to product liability claims if the use of our products is alleged to have resulted in injury.
−Removed: Our products consist of vitamins, minerals, herbs and other ingredients that are classified as food ingredients, dietary supplements, or natural health products, and, in most cases, are not subject to pre-market regulatory approval in the United States.
−Removed: Some of our products contain innovative ingredients that do not have long histories of human consumption.
−Removed: Previously unknown adverse reactions resulting from human consumption of these ingredients could occur.
−Removed: In addition, the products we sell are produced by third-party manufacturers.
−Removed: As a marketer of products manufactured by third parties, we also may be liable for various product liability claims for products we do not manufacture.
−Removed: We may, in the future, be subject to various product liability claims, including, among others, that our products include inadequate instructions for use or inadequate warnings concerning possible side effects and interactions with other substances.
−Removed: A product liability claim against us could result in increased costs and could adversely affect our reputation with our customers, which, in turn, could have a materially adverse effect on our business, results of operations, financial condition and cash flows.
−Removed: We utilize ingredients and components for our products from foreign suppliers, and may be negatively affected by the risks associated with international trade and importation issues .
−Removed: We utilize ingredients and components for a number of our products from suppliers outside of the United States.
−Removed: Accordingly, the acquisition of these ingredients is subject to the risks generally associated with importing raw materials, including, among other factors, delays in shipments, changes in economic and political conditions, quality assurance, health epidemics affecting the region of such suppliers, including COVID-19, nonconformity to specifications or laws and regulations, tariffs, trade disputes and foreign currency fluctuations.
−Removed: While we have a supplier certification program and audit and inspect our suppliers’ facilities as necessary both in the United States and internationally, we cannot assure you that raw materials received from suppliers outside of the United States will conform to all specifications, laws and regulations.
−Removed: There have in the past been quality and safety issues in our industry with certain items imported from overseas.
−Removed: We may incur additional expenses and experience shipment delays due to preventative measures adopted by the U.S.
−Removed: governments, our suppliers and our company.
−Removed: The insurance industry has become more selective in offering some types of coverage and we may not be able to obtain insurance coverage in the future .
−Removed: The insurance industry has become more selective in offering some types of insurance, such as product liability, product recall, property and directors’ and officers’ liability insurance.
−Removed: Our current insurance program is consistent with both our past level of coverage and our risk management policies.
−Removed: However, we cannot assure you that we will be able to obtain comparable insurance coverage on favorable terms, or at all, in the future.
−Removed: Certain of our customers as well as prospective customers require that we maintain minimum levels of coverage for our products.
−Removed: Lack of coverage or coverage below these minimum required levels could cause these customers to materially change business terms or to cease doing business with us entirely.
−Removed: If we experience product recalls, we may incur significant and unexpected costs, and our business reputation could be adversely affected.
−Removed: We may be exposed to product recalls and adverse public relations if our products are alleged to be mislabeled or to cause injury or illness, or if we are alleged to have violated governmental regulations.
−Removed: A product recall could result in substantial and unexpected expenditures, which would reduce operating profit and cash flow.
−Removed: In addition, a product recall may require significant management attention.
−Removed: Product recalls may hurt the value of our brands and lead to decreased demand for our products.
−Removed: Product recalls also may lead to increased scrutiny by federal, state or international regulatory agencies of our operations and increased litigation and could have a material adverse effect on our business, results of operations, financial condition and cash flows.
−Removed: *We depend on key personnel, the loss of any of which could negatively affect our business .
−Removed: We depend greatly on the collective services of Frank L.
−Removed: Jaksch Jr., Robert N.
−Removed: Fried, Kevin M.
−Removed: Farr, William Carter and Fadi Karam, who are our Executive Chairman of the Board, Chief Executive Officer, Chief Financial Officer, Senior Vice President of Business Affairs, and Chief Marketing Officer, respectively.
−Removed: We also depend greatly on other key employees, including key scientific and marketing personnel.
−Removed: In general, only highly qualified and trained scientists have the necessary skills to develop our products and provide our services.
−Removed: Only marketing personnel with specific experience and knowledge in health care are able to effectively market our products.
−Removed: In addition, some of our manufacturing, quality control, safety and compliance, information technology, sales and e-commerce related positions are highly technical as well.
−Removed: We face intense competition for these professionals from our competitors, customers, marketing partners and other companies throughout the industries in which we compete.
−Removed: Our success will depend, in part, upon our ability to attract and retain additional skilled personnel, which will require substantial additional funds.
−Removed: There can be no assurance that we will be able to find and attract additional qualified employees or retain any such personnel.
−Removed: Our inability to hire qualified personnel, the loss of services of our key personnel, or the loss of services of executive officers or key employees that may be hired in the future may have a material and adverse effect on our business.
−Removed: Our operating results may fluctuate significantly as a result of a variety of factors, many of which are outside of our control.
−Removed: We are subject to the following factors, among others, that may negatively affect our operating results:
−Removed: • the announcement or introduction of new products by our competitors;
−Removed: • our ability to upgrade and develop our systems and infrastructure to accommodate growth;
−Removed: • the decision by significant customers to reduce purchases;
−Removed: • disputes and litigation with competitors;
−Removed: • our ability to attract and retain key personnel in a timely and cost-effective manner;
−Removed: • technical difficulties;
−Removed: • the amount and timing of operating costs and capital expenditures relating to the expansion of our business, operations and infrastructure;
−Removed: • regulation by federal, state or local governments;
−Removed: • general economic conditions as well as economic conditions specific to the healthcare industry.
−Removed: For example, our operating results may be harmed by the effect of the COVID-19 pandemic on global economic conditions.
−Removed: As a result of our limited operating history and the nature of the markets in which we compete, it is extremely difficult for us to make accurate forecasts.
−Removed: We have based our current and future expense levels largely on our investment plans and estimates of future events although certain of our expense levels are, to a large extent, fixed.
−Removed: Assuming our products reach the market, we may be unable to adjust spending in a timely manner to compensate for any unexpected revenue shortfall.
−Removed: Accordingly, any significant shortfall in revenues relative to our planned expenditures would have an immediate adverse effect on our business, results of operations and financial condition.
−Removed: Further, as a strategic response to changes in the competitive environment, we may from time to time make certain pricing, service or marketing decisions that could have a material and adverse effect on our business, results of operations and financial condition.
−Removed: Due to the foregoing factors, our revenues and operating results are and will remain difficult to forecast.
We face significant competition, including changes in pricing.
15 unchanged sentences
In certain instances, competitors with greater financial resources also may be able to enter a market in direct competition with us, offering attractive marketing tools to encourage the sale of products that compete with our products or present cost features that consumers may find attractive.
−Removed: We may never develop any additional products to commercialize.
−Removed: We have invested a substantial amount of our time and resources in developing various new products.
−Removed: Commercialization of these products will require additional development, clinical evaluation, regulatory approval, significant marketing efforts and substantial additional investment before they can provide us with any revenue.
−Removed: Despite our efforts, these products may not become commercially successful products for a number of reasons, including but not limited to:
−Removed: • we may not be able to obtain regulatory approvals for our products, or the approved indication may be narrower than we seek;
−Removed: • our products may not prove to be safe and effective in clinical trials;
−Removed: • we may experience delays in our development program;
−Removed: • any products that are approved may not be accepted in the marketplace;
−Removed: • we may not have adequate financial or other resources to complete the development or to commence the commercialization of our products or will not have adequate financial or other resources to achieve significant commercialization of our products;
−Removed: • we may not be able to manufacture any of our products in commercial quantities or at an acceptable cost;
−Removed: • rapid technological change may make our products obsolete;
−Removed: • we may be unable to effectively protect our intellectual property rights or we may become subject to claims that our activities have infringed the intellectual property rights of others;
−Removed: • we may be unable to obtain or defend patent rights for our products.
−Removed: In addition, we may never achieve technical feasibility under the supply agreement with Nestec Ltd., and therefore our sales and profit expectations resulting from this agreement may be reduced.
−Removed: We may not be able to partner with others for technological capabilities and new products and services.
−Removed: Our ability to remain competitive may depend, in part, on our ability to continue to seek partners that can offer technological improvements and improve existing products and services that are offered to our customers.
−Removed: We are committed to attempting to keep pace with technological change, to stay abreast of technology changes and to look for partners that will develop new products and services for our customer base.
−Removed: We cannot assure prospective investors that we will be successful in finding partners or be able to continue to incorporate new developments in technology, to improve existing products and services, or to develop successful new products and services, nor can we be certain that newly developed products and services will perform satisfactorily or be widely accepted in the marketplace or that the costs involved in these efforts will not be substantial.
−Removed: If we fail to maintain adequate quality standards for our products and services, our business may be adversely affected and our reputation harmed.
−Removed: Dietary supplement, nutraceutical, food and beverage, functional food, analytical laboratories, pharmaceutical and cosmetic customers are often subject to rigorous quality standards to obtain and maintain regulatory approval of their products and the manufacturing processes that generate them.
−Removed: A failure to maintain, or, in some instances, upgrade our quality standards to meet our customers’ needs, could cause damage to our reputation and potentially result in substantial sales losses.
−Removed: We may be subject to damages resulting from claims that we, our employees, or our independent contractors have wrongfully used or disclosed alleged trade secrets of others.
−Removed: Some of our employees were previously employed at other dietary supplement, nutraceutical, food and beverage, functional food, analytical laboratories, pharmaceutical and cosmetic companies.
−Removed: We may also hire additional employees who are currently employed at other such companies, including our competitors.
−Removed: Additionally, consultants or other independent agents with which we may contract may be or have been in a contractual arrangement with one or more of our competitors.
−Removed: We may be subject to claims that these employees or independent contractors have used or disclosed such other party’s trade secrets or other proprietary information.
−Removed: Litigation may be necessary to defend against these claims.
−Removed: Even if we are successful in defending against these claims, litigation could result in substantial costs and be a distraction to our management.
−Removed: If we fail to defend such claims, in addition to paying monetary damages, we may lose valuable intellectual property rights or personnel.
−Removed: A loss of key personnel or their work product could hamper or prevent our ability to market existing or new products, which could severely harm our business.
Litigation may harm our business.
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Disputes from time to time with such companies, organizations or individuals are not uncommon, and we cannot assure you that we will always be able to resolve such disputes on terms favorable to us.
−Removed: As further described in Part II, Item 1 of this Quarterly Report on Form 10-Q, we are currently involved in substantial and complex litigation.
+Added: As further described in Note 10, Commitments and Contingencies, Contingencies in the Notes to the Consolidated Financial Statements, included in Part I, Item 1 of this Quarterly Report on Form 10-Q, we are currently involved in substantial and complex litigation.
Unexpected results could cause us to have financial exposure in these matters in excess of recorded reserves and insurance coverage, requiring us to provide additional reserves to address these liabilities, therefore impacting profits.
13 unchanged sentences
The timing of the receipt of grant funds may affect the timing of purchase decisions by our customers and, as a result, cause fluctuations in our sales and operating results.
−Removed: Demand for our products and services are subject to the commercial success of our customers’ products, which may vary for reasons outside our control.
−Removed: Even if we are successful in securing utilization of our products in a customer’s manufacturing process, sales of many of our products and services remain dependent on the timing and volume of the customer’s production, over which we have no control.
−Removed: The demand for our products depends on regulatory approvals and frequently depends on the commercial success of the customer’s supported product.
−Removed: Regulatory processes are complex, lengthy, expensive, and can often take years to complete.
+Added: Risks Related to our Operations
+Added: We depend on key personnel, the loss of any of which could negatively affect our business .
+Added: We depend greatly on the collective services of Frank L.
+Added: Jaksch Jr., Robert N.
+Added: Fried and Kevin M.
+Added: Farr, who are our Executive Chairman of the Board, Chief Executive Officer and Chief Financial Officer, respectively.
+Added: We also depend greatly on other key employees, including key scientific and marketing personnel.
+Added: In general, only highly qualified and trained scientists have the necessary skills to develop our products and provide our services.
+Added: Only marketing personnel with specific experience and knowledge in health care are able to effectively market our products.
+Added: In addition, some of our manufacturing, quality control, safety and compliance, information technology, sales and e-commerce related positions are highly technical as well.
+Added: We face intense competition for these professionals from our competitors, customers, marketing partners and other companies throughout the industries in which we compete.
+Added: Our success will depend, in part, upon our ability to attract and retain additional skilled personnel, which will require substantial additional funds.
+Added: There can be no assurance that we will be able to find and attract additional qualified employees or retain any such personnel.
+Added: Our inability to hire qualified personnel, the loss of services of our key personnel, or the loss of services of executive officers or key employees that may be hired in the future may have a material and adverse effect on our business.
+Added: Our operating results may fluctuate significantly as a result of a variety of factors, many of which are outside of our control.
+Added: We are subject to the following factors, among others, that may negatively affect our operating results:
+Added: • the announcement or introduction of new products by our competitors;
+Added: • our ability to upgrade and develop our systems and infrastructure to accommodate growth;
+Added: • the decision by significant customers to reduce purchases;
+Added: • disputes and litigation with competitors;
+Added: • our ability to attract and retain key personnel in a timely and cost-effective manner;
+Added: • technical difficulties;
+Added: • the amount and timing of operating costs and capital expenditures relating to the expansion of our business, operations and infrastructure;
+Added: • regulation by federal, state or local governments;
+Added: • general economic conditions as well as economic conditions specific to the healthcare industry.
+Added: For example, our operating results may be harmed by the effect of the COVID-19 pandemic on global economic conditions.
+Added: As a result of our limited operating history and the nature of the markets in which we compete, it is extremely difficult for us to make accurate forecasts.
+Added: We have based our current and future expense levels largely on our investment plans and estimates of future events although certain of our expense levels are, to a large extent, fixed.
+Added: Assuming our products reach the market, we may be unable to adjust spending in a timely manner to compensate for any unexpected revenue shortfall.
+Added: Accordingly, any significant shortfall in revenues relative to our planned expenditures would have an immediate adverse effect on our business, results of operations and financial condition.
+Added: Further, as a strategic response to changes in the competitive environment, we may from time to time make certain pricing, service or marketing decisions that could have a material and adverse effect on our business, results of operations and financial condition.
+Added: Due to the foregoing factors, our revenues and operating results are and will remain difficult to forecast.
+Added: We may need to increase the size of our organization, and we can provide no assurance that we will successfully expand operations or manage growth effectively.
+Added: Our significant increase in the scope and the scale of our product launches, including the hiring of additional personnel, has resulted in significantly higher operating expenses.
+Added: As a result, we anticipate that our operating expenses will continue to increase.
+Added: Expansion of our operations may also cause a significant demand on our management, finances and other resources.
+Added: Our ability to manage the anticipated future growth, should it occur, will depend upon a significant expansion of our accounting and other internal management systems and the implementation and subsequent improvement of a variety of systems, procedures and controls.
+Added: There can be no assurance that significant problems in these areas will not occur.
+Added: Any failure to expand these areas and implement and improve such systems, procedures and controls in an efficient manner at a pace consistent with our business could have a material adverse effect on our business, financial condition and results of operations.
+Added: There can be no assurance that our attempts to expand our marketing, sales, manufacturing and customer support efforts will be successful or will result in additional sales or profitability in any future period.
+Added: As a result of the expansion of our operations and the anticipated increase in our operating expenses, as well as the difficulty in forecasting revenue levels, we expect to continue to experience significant fluctuations in our results of operations.
+Added: The insurance industry has become more selective in offering some types of coverage and we may not be able to obtain insurance coverage in the future.
+Added: The insurance industry has become more selective in offering some types of insurance, such as product liability, product recall, property and directors’ and officers’ liability insurance.
+Added: Our current insurance program is consistent with both our past level of coverage and our risk management policies.
+Added: However, we cannot assure you that we will be able to obtain comparable insurance coverage on favorable terms, or at all, in the future.
+Added: Certain of our customers as well as prospective customers require that we maintain minimum levels of coverage for our products.
+Added: Lack of coverage or coverage below these minimum required levels could cause these customers to materially change business terms or to cease doing business with us entirely.
We may bear financial risk if we underprice our contracts or overrun cost estimates.
1 unchanged sentence
Such underpricing or significant cost overruns could have a material adverse effect on our business, results of operations, financial condition and cash flows.
−Removed: We rely on single or a limited number of third-party suppliers for the raw materials required to produce our products.
−Removed: Our dependence on a limited number of third-party suppliers or on a single supplier, and the challenges we may face in obtaining adequate supplies of raw materials, involve several risks, including limited control over pricing, availability, health epidemics affecting the region of such suppliers (including the coronavirus), quality and delivery schedules.
−Removed: We cannot be certain that our current suppliers will continue to provide us with the quantities of these raw materials that we require or satisfy our anticipated specifications and quality requirements.
−Removed: Due to COVID-19, there may be delays in shipments from our suppliers.
−Removed: Any supply interruption in limited or sole sourced raw materials could materially harm our ability to manufacture our products until a new source of supply, if any, could be identified and qualified.
−Removed: We may be unable to find a sufficient alternative supply channel in a reasonable time or on commercially reasonable terms.
−Removed: Any performance failure on the part of our suppliers could delay the development and commercialization of our products, or interrupt production of then existing products that are already marketed, which would have a material adverse effect on our business.
−Removed: For example, W.R.
−Removed: Grace & Co.-Conn.
−Removed: (Grace) is the exclusive manufacturer to us for the supply of NR.
−Removed: There is no guarantee that we will be able to continue to contract with Grace for the supply of NR, or that such terms will be favorable to us.
We may not be successful in acquiring complementary businesses or products on favorable terms.
22 unchanged sentences
If we are unable to establish and maintain adequate sales, marketing and distribution capabilities, independently or with others, we will not be able to generate product revenue, and may not become profitable.
+Added: Our failure to establish and maintain effective internal control over financial reporting could result in material misstatements in our financial statements, our failure to meet our reporting obligations and cause investors to lose confidence in our reported financial information, which in turn could cause the trading price of our common stock to decline.
+Added: Maintaining effective internal control over financial reporting is necessary for us to produce reliable and timely financial statements and disclosures.
+Added: If we identify material weaknesses in our internal controls and/or fail to establish and maintain effective controls and procedures and internal control over financial reporting it could result in material misstatements in our financial statements and/or a failure to meet our reporting and financial obligations, each of which could have a material adverse effect on our financial condition and the trading price of our common stock.
+Added: We are subject to financial and operating covenants in our business financing agreement with Western Alliance Bank, as amended (Credit Agreement) and any failure to comply with such covenants, or obtain waivers in the event of non-compliance, could limit our borrowing availability under the Credit Agreement, resulting in our being unable to borrow under the Credit Agreement and materially adversely impact our liquidity.
+Added: In addition, our operations may not provide sufficient cash to meet the repayment obligations of debt incurred under the Credit Agreement.
+Added: The Credit Agreement contains affirmative and restrictive covenants, including covenants regarding delivery of financial statements, maintenance of inventory, payment of taxes, maintenance of insurance, dispositions of property, business combinations or acquisitions and incurrence of additional indebtedness, among other customary covenants, in each case subject to limited exceptions.
+Added: There can be no assurance that we will be able to comply with the financial and other covenants in the Credit Agreement, and the effects of COVID-19 may make it more difficult for us to comply with such covenants.
+Added: Our failure to comply with these covenants could cause us to be unable to borrow under the Credit Agreement and may constitute an event of default which, if not cured or waived, could result in the acceleration of the maturity of any indebtedness then outstanding under the Credit Agreement, which would require us to pay all amounts then outstanding.
+Added: If we are unable to repay those amounts, Western Alliance Bank could proceed against the collateral granted to them to secure that debt, which would seriously harm our business.
+Added: Such an event could materially adversely affect our financial condition and liquidity.
+Added: Additionally, such events of non-compliance could impact the terms of any additional borrowings and/or any credit renewal terms.
+Added: Any failure to comply with such covenants may be a disclosable event and may be perceived negatively.
+Added: Such perception could adversely affect the market price for our common stock and our ability to obtain financing in the future.
Our business could be negatively impacted by cyber security threats, including without limitation a material interruption to our operations including our clinical trials, harm to our reputation, significant fines, penalties and liabilities, breach or triggering of data protection laws, privacy policies and data protection obligations, or a loss of customers or sales.
1 unchanged sentence
We use our data centers and our networks, and those of third parties, to store and access our proprietary business and other sensitive information.
−Removed: We face various cyber security threats, which are prevalent and continue to increase, including cyber security attacks to our information technology infrastructure and attempts by others to gain access to our proprietary or sensitive information.
−Removed: Due to COVID-19, there may be additional cyber security threats as most of our employees work from home, utilizing network connections outside of the Company premises.
−Removed: Information security risks have significantly increased in recent years in part due to the proliferation of new technologies and the increased sophistication and activities of organized crime, hackers, data and related privacy breaches, terrorists and other external parties, including foreign private parties and state and state-sponsored actors.
−Removed: Despite the implementation of preventative and detective security measures, our internal computer systems and those of our current and any future contractors, consultants, collaborators and third-party service providers, are vulnerable to damage or interruption from a variety of sources, including computer viruses, worms, software bugs, employee theft or misuse, other unauthorized access, software or hardware failures, server malfunctions, accidental acts or omissions by those with authorized access, natural disasters, terrorism, war, telecommunication and electrical failure, and cybersecurity threats (including the deployment of harmful malware, ransomware, denial-of-service attacks (such as credential stuffing), supply chain attacks, social engineering, and other means to affect service reliability and threaten the confidentiality, integrity, and availability of information).
−Removed: Ransomware attacks, including those from organized criminal threat actors, nation-states and nation-state supported actors, are becoming increasingly prevalent and severe and can lead to significant interruptions, delays, or outages in our operations, disruption of clinical trials, loss of data (including data related to clinical trials), loss of income, significant extra expenses to restore data or systems, reputational loss and the diversion of funds.
+Added: We and the third parties upon which we rely may face various cyber security threats, which are prevalent and continue to increase, including, without limitation, cyber security attacks to our information technology infrastructure and attempts by others to gain access to our proprietary or sensitive information, social-engineering attacks (including through phishing attacks), malicious code (such as viruses and worms), malware (including as a result of advanced persistent threat intrusions), denial-of-service attacks (such as credential stuffing), personnel misconduct or error, ransomware attacks, supply-chain attacks, software bugs, server malfunctions, software or hardware failures, loss of data or other information technology assets, adware, telecommunications failures, earthquakes, fires, floods, and other similar threats.
+Added: We rely upon third parties service providers and technologies to operate critical business systems to process confidential and personal information in a variety of contexts, including, without limitation, third-party providers of cloud-based infrastructure, employee email, and other functions.
+Added: Our ability to monitor these third-party providers information security practices is limited, and these third-parties may not have adequate information security measures in place.
+Added: Ransomware attacks, including those from organized criminal threat actors, nation-states and nation-state supported actors, are becoming increasingly prevalent and can lead to significant interruptions, delays, or outages in our operations, disruption of clinical trials, loss of data (including data related to clinical trials), loss of income, significant extra expenses to restore data or systems, reputational loss and the diversion of funds.
To alleviate the financial, operational and reputational impact of a ransomware attack it may be preferable to make extortion payments, but we may be unwilling or unable to do so (including, for example, if applicable laws or regulations prohibit such payments).
−Removed: The procedures and controls we use to monitor these threats and mitigate our exposure may not be sufficient to prevent all security incidents.
+Added: Similarly, supply-chain attacks have increased in frequency and severity, and we cannot guarantee that third-parties and infrastructure in our supply chain or our third-party partners’ supply-chains have not been compromised or that they do not contain exploitable defects or bugs that could result in a breach of or disruption to our information technology systems (including our products/services) or the third-party information technology systems that support us and our services.
+Added: Due to COVID-19, there may be additional cyber security threats as most of our employees work from home, utilizing network connections outside of the Company premises.
+Added: These information security risks have significantly increased in recent years in part due to the proliferation of new technologies and the increased sophistication and activities of organized crime, hackers, data and related privacy breaches, terrorists and other external parties, including foreign private parties and state and state-sponsored actors.
+Added: Any of the previously identified or similar threats could cause a security incident or other interruption and could result in unauthorized, unlawful, or accidental acquisition, modification, destruction, loss, alteration, encryption, disclosure of, or access to data.
+Added: A security incident or other interruption could disrupt our ability (and that of third parties upon whom we rely) to provide our products and services.
+Added: Despite the implementation of preventative and detective security measures designed to protect against security incidents, there can be no assurance that these measures will be effective and our internal computer systems and those of our current and any future contractors, consultants, collaborators and third-party service providers, may be vulnerable to damage or interruption from a variety of sources.
+Added: We may be unable to detect vulnerabilities in our information technology systems (including our products) because such threats and techniques change frequently, are often sophisticated in nature, and may not be detected until after a security incident has occurred.
+Added: Despite our efforts to identify and remediate vulnerabilities, if any, in our information technology systems (including our products), our efforts may not be successful.
+Added: Further, we may experience delays in developing and deploying remedial measures designed to address any such identified vulnerabilities.
+Added: The procedures and controls we use to monitor these vulnerabilities and threats and to mitigate our exposure may not be sufficient to prevent all security incidents.
These incidents could result in disrupted operations, including suspension of our clinical trial activities, lost opportunities, misstated financial data, liability for stolen assets or information, theft of our intellectual property, loss of data and other personally identifiable or sensitive information, increased costs arising from the implementation of additional security protective measures, litigation and reputational damage.
We may expend significant resources, fundamentally change our business activities and practices, or modify our operations, including our clinical trial activities, or information technology in an effort to protect against security incidents and to mitigate, detect, and remediate actual and potential vulnerabilities.
−Removed: If we, or a third party upon whom we rely, experience a security incident, or are perceived to have experienced a security incident, it may result in:
+Added: An actual or perceived security incident suffered by us or by a third party upon whom we rely may result in:
government enforcement actions that could include investigations, fines, penalties, audits and inspections;
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or orders to destroy or not use personal data;
−Removed: Further, individuals or other relevant stakeholders could sue us for our actual or perceived failure to comply with our security obligations, including, without limitation, in class action litigation.
−Removed: Security incidents could also result in indemnity obligations, negative publicity and financial loss.
−Removed: Security incidents and vulnerabilities may cause some of our customers and users to stop using our services and our failure, or perceived failure, to meet expectations with regard to the security, integrity, availability and confidentiality of our systems and sensitive data could damage our reputation and affect our ability to retain customers, attract new customers and grow our business.
−Removed: Moreover, security incidents can result in the diversion of funds and interruptions, delays, or outages in our operations and services, including due to ransomware attacks.
+Added: indemnification obligations;
+Added: negative publicity;
+Added: reputational harm;
+Added: monetary fund diversions;
+Added: interruptions in our operations (including availability of data);
+Added: financial loss;
+Added: and other similar harms.
+Added: Further, individuals, clinical trial participants or other relevant stakeholders could sue us for our actual or perceived failure to comply with our security obligations, including, without limitation, in class action litigation.
+Added: These proceedings could force us to spend money in defense or settlement, divert management’s time and attention, increase our costs of doing business, adversely affect our reputation or otherwise adversely affect our business.
+Added: Security incidents and vulnerabilities may cause some of our customers and users to stop using our services and our failure, or perceived failure, to meet expectations with regard to the security, integrity, availability and confidentiality of our network systems and sensitive data could damage our reputation and affect our ability to retain customers, attract new customers and grow our business.
+Added: Moreover, security incidents can result in the diversion of funds and interruptions, delays, or outages in our operations and services, including due to ransomware attacks and denial-of-service attacks.
Failures or significant downtime of our information technology or telecommunication systems or those used by our third-party service providers could cause significant interruptions in our operations and adversely impact the confidentiality, integrity and availability of sensitive or confidential information, including preventing us from conducting clinical trials, tests or research and development activities and preventing us from managing the administrative aspects of our business.
+Added: Additionally, some applicable federal, state and foreign laws may require companies to notify individuals of security breaches involving particular personally identifiable information, which could result from breaches experienced by us or by our vendors, contractors, or organizations with which we have relationships.
+Added: Notifications and follow-up actions related to a security breach are costly, and the disclosures or the failure to comply with such requirements could lead to adverse consequences and could impact our reputation or cause us to incur significant costs, including legal expenses and remediation costs.
Any remedial costs or other liabilities related to security incidents may not be fully insured or indemnified by other means.
−Removed: Additionally, some of the federal, state and foreign government requirements include obligations for companies to notify individuals of security breaches involving particular personally identifiable information, which could result from breaches experienced by us or by our vendors, contractors, or organizations with which we have relationships.
−Removed: Notifications and follow-up actions related to a security breach could impact our reputation or cause us to incur significant costs, including legal expenses and remediation costs.
−Removed: Compliance with stringent and changing global privacy and data security requirements could result in additional costs and liabilities to us or inhibit our ability to collect and, if applicable, process data globally, and the failure or perceived failure to comply with such requirements could have a material adverse effect on our business, financial condition or results of operations.
−Removed: We collect, receive, store, process, use, generate, transfer, disclose, make accessible, protect and share personal information and other sensitive information, including but not limited to proprietary and confidential business information, trade secrets, intellectual property, information we collect about patients in connection with clinical trials, and sensitive third-party information necessary to operate our business, for legal and marketing purposes.
−Removed: Accordingly, we are, or may become, subject to numerous federal, state, local, and foreign data privacy and security laws, regulations, guidance and industry standards as well as external and internal privacy and security policies, contracts and other obligations that apply to the processing of personal data by us and on our behalf.
−Removed: The legal framework for the collection, use, safeguarding, sharing, transfer and other processing of information worldwide is rapidly evolving and may remain unsettled for the foreseeable future.
−Removed: For example, the European Union’s General Data Protection Regulation (GDPR) imposes strict obligations on the processing of personal data, including, without limitation, personal health data, and the free movement of such data.
−Removed: The GDPR applies to any company established in the European Union as well as any company outside the European Union that processes personal data in connection with the offering of goods or services to individuals in the European Union or the monitoring of their behavior.
−Removed: The GDPR imposes data protection obligations on processors and controllers of personal data, including, for example, obligations relating to:
−Removed: processing health and other sensitive data;
−Removed: obtaining consent of individuals;
−Removed: providing notice to individuals regarding data processing activities;
−Removed: responding to data subject requests;
−Removed: taking certain measures when engaging third-party processors;
−Removed: notifying data subjects and regulators of data breaches;
−Removed: implementing safeguards to protect the security and confidentiality of personal data;
−Removed: and transferring personal data to countries outside the European Union, including the United States.
−Removed: The GDPR imposes fines for breaches of data protection requirements and provides other remedies for parties who suffer harm as a result of a data breach.
−Removed: Furthermore, the vote in the United Kingdom in favor of exiting the European Union, referred to as Brexit, has complicated data protection regulation in the United Kingdom.
−Removed: As of January 1, 2021, the GDPR has been converted into United Kingdom law and the United Kingdom is now a “third country” under the GDPR.
−Removed: The GDPR and other changes in laws or regulations associated with the enhanced protection of certain types of sensitive data, such as healthcare data or other personal information from our clinical trials, could require us to change our business practices or lead to government enforcement actions, private litigation or significant penalties against us and could have a material adverse effect on our business, financial condition or results of operations.
−Removed: Similarly, European data protection laws also generally prohibit the transfer of personal data from Europe to countries outside the European Economic Area (EEA), such as the United States, unless the parties to the transfer have implemented specific safeguards to protect the transferred personal data.
−Removed: One of the primary safeguards used for transfers of personal data from the European Union to the United States, namely, the Privacy Shield framework administered by the U.S.
−Removed: Department of Commerce, was recently invalidated by a decision of the European Union’s highest court.
−Removed: The same decision also cast doubt on the ability to use one of the primary alternatives to the Privacy Shield, namely, the European Commission’s Standard Contractual Clauses, to lawfully transfer personal data from Europe to the United States and most other countries.
−Removed: On June 4, 2021, the European Commission adopted new standard contractual clauses (SCCs) under the GDPR for personal data transfers outside the EEA.
−Removed: Under this legal mechanism, we may have obligations to conduct transfer impact assessments for such cross-border data transfers and implement additional security measures.
−Removed: We have and may elect to continue to rely on the new SCCs, which have and may require us to expend significant resources to comply with such obligations, and where needed, to update our contractual arrangements.
−Removed: In addition, Swiss and English law contain similar data transfer restrictions as the GDPR, and the Swiss Federal Data Protection and Information Commissioner recently opined that the Swiss-U.S.
−Removed: Privacy Shield may also be inadequate for transfers of data from Switzerland to the United States.
−Removed: As for the United Kingdom, on June 28, 2021, the European Commission issued an adequacy decision under the GDPR which allows transfers (other than those carried out for the purposes of United Kingdom immigration control) of personal data from the EEA to the United Kingdom to continue without restriction for a period of four years ending June 27, 2025.
−Removed: After that period, the adequacy decision may be renewed, however, only if the United Kingdom continues to ensure an adequate level of data protection.
−Removed: During these four years, the European Commission will continue to monitor the legal situation in the United Kingdom and could intervene at any point if the United Kingdom deviates from the level of data protection in place at the time of issuance of the adequacy decision.
−Removed: If the adequacy decision is withdrawn or not renewed, transfers of personal data from the EEA to the United Kingdom will require a valid ‘transfer mechanism,’ and we may be required to implement new processes and put new agreements in place, such as SCCs, to enable transfers of personal data from the EEA to the United Kingdom to continue.
−Removed: If we are unable to implement a valid compliance mechanism for cross-border personal information transfers, we may face increased exposure to regulatory actions, substantial fines and injunctions against processing or transferring personal information from Europe or elsewhere.
−Removed: Inability to import personal information from Europe or elsewhere to the United States may significantly and negatively impact our business operations, including by limiting our ability to conduct clinical trial activities in Europe and elsewhere;
−Removed: limiting our ability to collaborate with Contract Research Organizations, service providers, contractors and other companies subject to European and other data protection laws;
−Removed: or requiring us to increase our data processing capabilities in Europe or elsewhere at significant expense.
−Removed: Additionally, we are, or may become, subject to U.S.
−Removed: privacy laws.
−Removed: For example, the California Consumer Privacy Act (CCPA) creates new individual privacy rights for consumers and places increased privacy and security obligations on entities handling personal data of consumers.
−Removed: Among other things, the CCPA requires covered companies to provide new disclosures to California consumers and provides such consumers new ways to opt-out of certain sales of personal information.
−Removed: The CCPA provides for penalties for violations, as well as other remedies for parties who suffer harm as a result of a data breach, which may increase data breach litigation.
−Removed: Moreover, effective starting on January 1, 2023, the California Privacy Rights Act (CPRA) will significantly modify the CCPA, including by expanding consumers’ rights with respect to certain sensitive personal information.
−Removed: The CPRA also creates a new state agency that will be vested with authority to implement and enforce the CCPA and the CPRA.
−Removed: Although there are limited exemptions for clinical trial data under the CCPA, the CCPA and other similar laws could impact our business activities depending on how they are interpreted.
−Removed: In addition, other states have enacted or proposed data privacy laws, which could further complicate the legal landscape.
−Removed: For example, Virginia recently passed its Consumer Data Protection Act, and Colorado recently passed the Colorado Privacy Act, both effective 2023.
−Removed: Collectively, these laws may increase our compliance costs and potential liability.
−Removed: Although we endeavor to comply with our published policies, other documentation, and all applicable privacy and security laws, we may at times fail to do so or may be perceived to have failed to do so.
−Removed: If we fail, or are perceived to have failed, to address or comply with obligations related to data privacy and security, we could face government enforcement actions that could include investigations, fines, penalties, audits and inspections;
−Removed: additional reporting requirements and/or oversight;
−Removed: temporary or permanent bans on all or some processing of personal data;
−Removed: orders to destroy or not use personal data;
−Removed: and imprisonment of company officials.
−Removed: Further, individuals or other relevant stakeholders could sue us for our actual or perceived failure to comply with our data privacy and security obligations, including, without limitation, in class action litigation.
−Removed: Any of these events could have a material adverse effect on our reputation, business, or financial condition, and could lead to a loss of actual or prospective customers, collaborators or partners;
−Removed: interrupt or stop clinical trials;
−Removed: result in an inability to process personal data or to operate in certain jurisdictions;
−Removed: limit our ability to develop or commercialize our products;
−Removed: or require us to revise or restructure our operations.
−Removed: Moreover, such suits, even if we are not found liable, could be expensive and time-consuming to defend and could result in adverse publicity that could harm our business or have other material adverse effects.
−Removed: Additionally, we expect that there will continue to be new proposed laws and regulations concerning data privacy and security, and we cannot yet determine the impact such future laws, regulations and standards may have on our business.
−Removed: *Our failure to establish and maintain effective internal control over financial reporting could result in material misstatements in our financial statements, our failure to meet our reporting obligations and cause investors to lose confidence in our reported financial information, which in turn could cause the trading price of our common stock to decline.
−Removed: Maintaining effective internal control over financial reporting is necessary for us to produce reliable financial statements.
−Removed: Our management previously identified a material weakness in our internal control over financial reporting and concluded that the material weakness has not been remediated and our disclosure controls and procedures were not effective as of September 30, 2021.
−Removed: The material weakness in internal control over financial reporting resulted from a deficiency in our disclosure controls and procedures which could have resulted in us not disclosing a material potential loss requiring a qualitative disclosure and recording a liability in our consolidated financial statements under ASC 450 - Contingencies.
−Removed: If not remediated, or if we identify further material weaknesses in our internal controls, our failure to establish and maintain effective disclosure controls and procedures and internal control over financial reporting could result in material misstatements in our financial statements and a failure to meet our reporting and financial obligations, each of which could have a material adverse effect on our financial condition and the trading price of our common stock.
−Removed: We are subject to financial and operating covenants in our business financing agreement with Western Alliance Bank (Credit Agreement) and any failure to comply with such covenants, or obtain waivers in the event of non-compliance, could limit our borrowing availability under the Credit Agreement, resulting in our being unable to borrow under the Credit Agreement and materially adversely impact our liquidity.
−Removed: In addition, our operations may not provide sufficient cash to meet the repayment obligations of debt incurred under the Credit Agreement.
−Removed: The Credit Agreement contains affirmative and restrictive covenants, including covenants regarding delivery of financial statements, maintenance of inventory, payment of taxes, maintenance of insurance, dispositions of property, business combinations or acquisitions and incurrence of additional indebtedness, among other customary covenants, in each case subject to limited exceptions.
−Removed: There can be no assurance that we will be able to comply with the financial and other covenants in the Credit Agreement, and the effects of COVID-19 may make it more difficult for us to comply with such covenants.
−Removed: Our failure to comply with these covenants could cause us to be unable to borrow under the Credit Agreement and may constitute an event of default which, if not cured or waived, could result in the acceleration of the maturity of any indebtedness then outstanding under the Credit Agreement, which would require us to pay all amounts then outstanding.
−Removed: If we are unable to repay those amounts, Western Alliance Bank could proceed against the collateral granted to them to secure that debt, which would seriously harm our business.
−Removed: Such an event could materially adversely affect our financial condition and liquidity.
−Removed: Additionally, such events of non-compliance could impact the terms of any additional borrowings and/or any credit renewal terms.
−Removed: Any failure to comply with such covenants may be a disclosable event and may be perceived negatively.
−Removed: Such perception could adversely affect the market price for our common stock and our ability to obtain financing in the future.
+Added: Our contracts may not contain limitations of liability;
+Added: however, even where they do, there can be no assurance that limitations of liability in our contracts are sufficient to protect us from liabilities, damages, or claims related to our data privacy and security obligations.
+Added: Although we maintain cyber insurance, we cannot be sure that our insurance coverage will be adequate or sufficient of protect us from or to mitigate liabilities arising out of our privacy and security practices, that such coverage will continue to be available on commercially reasonable terms or at all, or that such coverage will pay future claims.
+Added: Risks Related to Our Products
+Added: Unfavorable publicity or consumer perception of our products and any similar products distributed by other companies could have a material adverse effect on our business.
+Added: We believe the nutritional supplement market is highly dependent upon consumer perception regarding the safety, efficacy and quality of nutritional supplements generally, as well as of products distributed specifically by us.
+Added: Consumer perception of our products can be significantly influenced by scientific research or findings, regulatory investigations, litigation, national media attention and other publicity regarding the consumption of nutritional supplements.
+Added: We cannot assure you that future scientific research, findings, regulatory proceedings, litigation, media attention or other favorable research findings or publicity will be favorable to the nutritional supplement market or any product, or consistent with earlier publicity.
+Added: Future research reports, findings, regulatory proceedings, litigation, media attention or other publicity that are perceived as less favorable than, or that question, such earlier research reports, findings or publicity could have a material adverse effect on the demand for our products and consequently on our business, results of operations, financial condition and cash flows.
+Added: Our dependence upon consumer perceptions means that adverse scientific research reports, findings, regulatory proceedings, litigation, media attention or other publicity, if accurate or with merit, could have a material adverse effect on the demand for our products, the availability and pricing of our ingredients, and our business, results of operations, financial condition and cash flows.
+Added: Further, adverse public reports or other media attention regarding the safety, efficacy and quality of nutritional supplements in general, or our products specifically, or associating the consumption of nutritional supplements with illness, could have such a material adverse effect.
+Added: Any such adverse public reports or other media attention could arise even if the adverse effects associated with such products resulted from consumers’ failure to consume such products appropriately or as directed and the content of such public reports and other media attention may be beyond our control.
+Added: We may incur material product liability claims, which could increase our costs and adversely affect our reputation, revenues and operating income .
+Added: As a consumer product and ingredient supplier we market and manufacture products designed for human and animal consumption.
+Added: We are subject to product liability claims if the use of our products is alleged to have resulted in injury.
+Added: Our products consist of ingredients classified as dietary supplements, or natural health products, and, in most cases, are not subject to pre-market regulatory approval in the United States.
+Added: Some of our products contain innovative ingredients that do not have long histories of human consumption.
+Added: Previously unknown adverse reactions resulting from human consumption of these ingredients could occur.
+Added: In addition, the products we sell are produced by third-party manufacturers.
+Added: As a marketer of products manufactured by third parties, we also may be liable for various product liability claims for products we do not manufacture.
+Added: We have, and may in the future, be subject to various product liability claims, including, among others, that our products include inadequate instructions for use or inadequate warnings concerning possible side effects and interactions with other substances.
+Added: A product liability claim against us could result in increased costs and could adversely affect our reputation with our customers, which, in turn, could have a materially adverse effect on our business, results of operations, financial condition and cash flows.
+Added: We utilize ingredients and components for our products from foreign suppliers, and may be negatively affected by the risks associated with international trade and importation issues.
+Added: We utilize ingredients and components for a number of our products from suppliers outside of the United States.
+Added: Accordingly, the acquisition of these ingredients is subject to the risks generally associated with importing raw materials, including, among other factors, delays in shipments, changes in economic and political conditions, quality assurance, health epidemics affecting the region of such suppliers, including COVID-19, nonconformity to specifications or laws and regulations, tariffs, trade and/or labor disputes and foreign currency fluctuations.
+Added: While we have a supplier certification program and audit and inspect our suppliers’ facilities as necessary both in the United States and internationally, we cannot assure you that raw materials received from suppliers outside of the United States will conform to all specifications, laws and regulations.
+Added: There have in the past been quality and safety issues in our industry with certain items imported from overseas.
+Added: We may incur additional expenses and experience shipment delays due to preventative measures adopted by the U.S.
+Added: governments, our suppliers and our company.
+Added: We may never develop any additional products to commercialize.
+Added: We have invested a substantial amount of our time and resources in developing various new products.
+Added: Commercialization of these products will require additional development, clinical evaluation, regulatory approval, significant marketing efforts and substantial additional investment before they can provide us with any revenue.
+Added: Despite our efforts, these products may not become commercially successful products for a number of reasons, including but not limited to:
+Added: • we may not be able to obtain regulatory approvals for our products, or the approved indication may be narrower than we seek;
+Added: • our products may not prove to be safe and effective in clinical trials;
+Added: • we may experience delays in our development program;
+Added: • any products that are approved may not be accepted in the marketplace;
+Added: • we may not have adequate financial or other resources to complete the development or to commence the commercialization of our products or will not have adequate financial or other resources to achieve significant commercialization of our products;
+Added: • we may not be able to manufacture any of our products in commercial quantities or at an acceptable cost;
+Added: • rapid technological change may make our products obsolete;
+Added: • we may be unable to effectively protect our intellectual property rights or we may become subject to claims that our activities have infringed the intellectual property rights of others;
+Added: • we may be unable to obtain or defend patent rights for our products.
+Added: In addition, we have a supply agreement with Nestec Ltd.
+Added: pursuant to which it is our exclusive customer for Niagen® for human use in the medical nutritional and functional food and beverage categories in certain territories.
+Added: We may never achieve technical feasibility under the supply agreement with Nestec Ltd., and therefore our sales and profit expectations resulting from this agreement may be reduced.
+Added: We may not be able to partner with others for technological capabilities and new products and services.
+Added: Our ability to remain competitive may depend, in part, on our ability to continue to seek partners that can offer technological improvements and improve existing products and services that are offered to our customers.
+Added: We are committed to attempting to keep pace with technological change, to stay abreast of technology changes and to look for partners that will develop new products and services for our customer base.
+Added: We cannot assure prospective investors that we will be successful in finding partners or be able to continue to incorporate new developments in technology, to improve existing products and services, or to develop successful new products and services, nor can we be certain that newly developed products and services will perform satisfactorily or be widely accepted in the marketplace or that the costs involved in these efforts will not be substantial.
+Added: If we fail to maintain adequate quality standards for our products and services, our business may be adversely affected and our reputation harmed.
+Added: Dietary supplement, nutraceutical, food and beverage, functional food, analytical laboratories, pharmaceutical and cosmetic customers are often subject to rigorous quality standards to obtain and maintain regulatory approval of their products and the manufacturing processes that generate them.
+Added: A failure to maintain, or, in some instances, upgrade our quality standards to meet our customers’ needs, could cause damage to our reputation and potentially result in substantial sales losses.
+Added: If we experience product recalls, we may incur significant and unexpected costs, and our business reputation could be adversely affected.
+Added: We may be exposed to product recalls and adverse public relations if our products are alleged to be mislabeled or to cause injury or illness, or if we are alleged to have violated governmental regulations.
+Added: A product recall could result in substantial and unexpected expenditures, which would reduce operating profit and cash flow.
+Added: In addition, a product recall may require significant management attention.
+Added: Product recalls may hurt the value of our brands and lead to decreased demand for our products.
+Added: Product recalls also may lead to increased scrutiny by federal, state or international regulatory agencies of our operations and increased litigation and could have a material adverse effect on our business, results of operations, financial condition and cash flows.
+Added: Demand for our products and services are subject to the commercial success of our customers’ products, which may vary for reasons outside our control.
+Added: Even if we are successful in securing utilization of our products in a customer’s manufacturing process, sales of many of our products and services remain dependent on the timing and volume of the customer’s production, over which we have no control.
+Added: The demand for our products depends on regulatory approvals and frequently depends on the commercial success of the customer’s supported product.
+Added: Regulatory processes are complex, lengthy, expensive, and can often take years to complete.
+Added: We rely on single or a limited number of third-party suppliers for the raw materials required to produce our products.
+Added: Our dependence on a limited number of third-party suppliers or on a single supplier, and the challenges we may face in obtaining adequate supplies of raw materials, involve several risks, including limited control over pricing, availability, health epidemics affecting the region of such suppliers (including the coronavirus), quality and delivery schedules.
+Added: We cannot be certain that our current suppliers will continue to provide us with the quantities of these raw materials that we require or satisfy our anticipated specifications and quality requirements.
+Added: Due to COVID-19, there may be delays in shipments from our suppliers.
+Added: Any supply interruption in limited or sole sourced raw materials could materially harm our ability to manufacture our products until a new source of supply, if any, could be identified and qualified.
+Added: We may be unable to find a sufficient alternative supply channel in a reasonable time or on commercially reasonable terms.
+Added: Any performance failure on the part of our suppliers could delay the development and commercialization of our products, or interrupt production of then existing products that are already marketed, which would have a material adverse effect on our business.
+Added: For example, W.R.
+Added: Grace & Co.-Conn.
+Added: (Grace) is the exclusive manufacturer to us for the supply of NR.
+Added: There is no guarantee that we will be able to continue to contract with Grace for the supply of NR, or that such terms will be favorable to us.
+Added: Risks Related to our Intellectual Property
+Added: Our ability to protect our intellectual property and proprietary technology through patents and other means is uncertain and may be inadequate, which would have a material and adverse effect on us.
+Added: Our success depends significantly on our ability to protect our proprietary rights to the technologies used in our products.
+Added: We rely on patent protection, as well as a combination of copyright, trade secret and trademark laws and nondisclosure, confidentiality and other contractual restrictions to protect our proprietary technology, including our licensed technology.
+Added: However, these legal means afford only limited protection and may not adequately protect our rights or permit us to gain or keep any competitive advantage.
+Added: For example, our pending United States and foreign patent applications may not issue as patents in a form that will be advantageous to us or may issue and be subsequently successfully challenged by others and invalidated.
+Added: In addition, our pending patent applications include claims to material aspects of our products and procedures that are not currently protected by issued patents.
+Added: Both the patent application process and the process of managing patent disputes can be time consuming and expensive.
+Added: Competitors may be able to design around our patents or develop products which provide outcomes which are comparable or even superior to ours.
+Added: Steps that we have taken to protect our intellectual property and proprietary technology, including entering into confidentiality agreements and intellectual property assignment agreements with some of our officers, employees, consultants and advisors, may not provide us with meaningful protection for our trade secrets or other proprietary information in the event of unauthorized use or disclosure or other breaches of the agreements.
+Added: Furthermore, the laws of foreign countries may not protect our intellectual property rights to the same extent as do the laws of the United States.
+Added: In the event a competitor infringes our licensed or pending patent or other intellectual property rights, enforcing those rights may be costly, uncertain, difficult and time consuming.
+Added: Even if successful, litigation to enforce our intellectual property rights or to defend our patents against challenge could be expensive and time consuming and could divert our management’s attention.
+Added: We may not have sufficient resources to enforce our intellectual property rights or to defend our patents rights against a challenge.
+Added: The failure to obtain patents and/or protect our intellectual property rights could have a material and adverse effect on our business, results of operations and financial condition.
+Added: Our patents and licenses may be subject to challenge on validity grounds, and our patent applications may be rejected.
+Added: We rely on our patents, patent applications, licenses and other intellectual property rights to give us a competitive advantage.
+Added: Whether a patent is valid, or whether a patent application should be granted, is a complex matter of science and law, and therefore we cannot be certain that, if challenged, our patents, patent applications and/or other intellectual property rights would be upheld nor can we be certain we will prevail in an appeal.
+Added: If one or more of those patents, patent applications, licenses and other intellectual property rights are invalidated, rejected or found unenforceable and we are unable to reverse that finding through an appeal, that could reduce or eliminate any competitive advantage we might otherwise have had.
+Added: We may become subject to claims of infringement or misappropriation of the intellectual property rights of others, which could prohibit us from developing our products, require us to obtain licenses from third parties or to develop non-infringing alternatives and subject us to substantial monetary damages.
+Added: Third parties could, in the future, assert infringement or misappropriation claims against us with respect to products we develop.
+Added: Whether a product infringes a patent or misappropriates other intellectual property involves complex legal and factual issues, the determination of which is often uncertain.
+Added: Therefore, we cannot be certain that we have not infringed the intellectual property rights of others.
+Added: There may be third-party patents or patent applications with claims to materials, formulations, methods of manufacture or methods for use related to the use or manufacture of our products, and our potential competitors may assert that some aspect of our product infringes their patents.
+Added: Because patent applications may take years to issue, there also may be applications now pending of which we are unaware that may later result in issued patents upon which our products could infringe.
+Added: There also may be existing patents or pending patent applications of which we are unaware upon which our products may inadvertently infringe.
+Added: Any infringement or misappropriation claim could cause us to incur significant costs, place significant strain on our financial resources, divert management’s attention from our business and harm our reputation.
+Added: If the relevant patents in such claim were upheld as valid and enforceable and we were found to infringe them, we could be prohibited from manufacturing or selling any product that is found to infringe unless we could obtain licenses to use the technology covered by the patent or are able to design around the patent.
+Added: We may be unable to obtain such a license on terms acceptable to us, if at all, and we may not be able to redesign our products to avoid infringement, which could materially impact our revenue.
+Added: A court could also order us to pay compensatory damages for such infringement, plus prejudgment interest and could, in addition, treble the compensatory damages and award attorney fees.
+Added: These damages could be substantial and could harm our reputation, business, financial condition and operating results.
+Added: A court also could enter orders that temporarily, preliminarily or permanently enjoin us and our customers from making, using, or selling products, and could enter an order mandating that we undertake certain remedial activities.
+Added: Depending on the nature of the relief ordered by the court, we could become liable for additional damages to third parties.
+Added: The prosecution and enforcement of patents licensed to us by third parties are not within our control.
+Added: Without these technologies, our products may not be successful and our business would be harmed if the patents were infringed on or misappropriated without action by such third parties.
+Added: We have obtained licenses from third parties for patents and patent application rights related to ingredients and/or the products we are developing, allowing us to use intellectual property rights owned by or licensed to these third parties.
+Added: We do not control the maintenance, prosecution, enforcement or strategy for many of these patents or patent application rights and as such are dependent in part on the owners of the intellectual property rights to maintain their viability.
+Added: If any third-party licensor is unable to successfully maintain, prosecute or enforce the licensed patents and/or patent application rights related to our products, we may become subject to infringement or misappropriate claims or lose our competitive advantage.
+Added: Without access to these technologies or suitable design-around or alternative technology options, our ability to conduct our business could be impaired significantly.
+Added: We are currently engaged in substantial and complex litigation with Elysium Health, Inc.
+Added: and Elysium Health LLC (collectively, "Elysium"), the outcome of which could materially harm our business and financial results.
+Added: The litigation includes multiple complaints and counterclaims by us and Elysium in venues in California and New York, as well as a patent infringement complaint filed by the Company and Trustees of Dartmouth College.
+Added: For further details on this litigation, please refer to Note 10, Commitments and Contingencies, Legal Proceedings in the Notes to the Consolidated Financial Statements, included in Part I, Item 1 of this Quarterly Report on Form 10-Q.
+Added: The litigation is substantial and complex, and it has caused and could continue to cause us to incur significant costs, as well as distract our management over an extended period.
+Added: The litigation may substantially disrupt our business and we cannot assure you that we will be able to resolve the litigation on terms favorable to us.
+Added: If we are unsuccessful in resolving the litigation on favorable terms to us, we may be forced to pay compensatory and punitive damages and restitution for any royalty payments that we received from Elysium, which payments could materially harm our business, or be subject to other remedies, including injunctive relief.
+Added: We cannot predict the outcome of our litigation with Elysium, which could have any of the results described above or other results that could materially adversely affect our business.
+Added: We may be subject to damages resulting from claims that we, our employees, or our independent contractors have wrongfully used or disclosed alleged trade secrets of others.
+Added: Some of our employees were previously employed at other dietary supplement, nutraceutical, food and beverage, functional food, analytical laboratories, pharmaceutical and cosmetic companies.
+Added: We may also hire additional employees who are currently employed at other such companies, including our competitors.
+Added: Additionally, consultants or other independent agents with which we may contract may be or have been in a contractual arrangement with one or more of our competitors.
+Added: We may be subject to claims that these employees or independent contractors have used or disclosed such other party’s trade secrets or other proprietary information.
+Added: Litigation may be necessary to defend against these claims.
+Added: Even if we are successful in defending against these claims, litigation could result in substantial costs and be a distraction to our management.
+Added: If we fail to defend such claims, in addition to paying monetary damages, we may lose valuable intellectual property rights or personnel.
+Added: A loss of key personnel or their work product could hamper or prevent our ability to market existing or new products, which could severely harm our business.
Risks Related to Regulatory Approval of Our Products and Other Government Regulations
4 unchanged sentences
If we fail to comply with any of these regulations, we may be subject to fines or penalties, have to recall products and/or cease their manufacture and distribution, which would increase our costs and reduce our sales.
−Removed: As disclosed above, we received the Letter from the FDA and FTC in November 2020, and the Second Letter from the FTC in April 2021.
We are also subject to various federal, state, local and international laws and regulations that govern the handling, transportation, manufacture, use and sale of substances that are or could be classified as toxic or hazardous substances.
6 unchanged sentences
Changes in regulations or the enforcement practices of current regulations could have a negative impact on our customers and, in turn, our business.
−Removed: At this time, it is unknown how the FDA will interpret and to what extent it will enforce GMPs, and other regulations that will likely affect many of our customers.
+Added: At this time, it is unknown how the FDA will interpret and to what extent it will enforce Good Manufacturing Practices, and other regulations that will likely affect many of our customers.
These uncertainties may have a material impact on our results of operations, as lack of enforcement or an interpretation of the regulations that lessens the burden of compliance for the dietary supplement marketplace may cause a reduced demand for our products and services.
12 unchanged sentences
There can be no assurance that we will obtain regulatory approval of our proposed goods that may require it.
+Added: Compliance with stringent and changing global privacy and data security laws and regulations could result in additional costs and liabilities to us or inhibit our ability to collect and, if applicable, process data globally, and the failure or perceived failure to comply with such laws and regulations could have a material adverse effect on our business, financial condition or results of operations.
+Added: We collect, receive, store, process, use, generate, transfer, disclose, make accessible, protect and share personal information and other sensitive information, including but not limited to proprietary and confidential business information, trade secrets, intellectual property, information we collect about patients in connection with clinical trials, and sensitive third-party information necessary to operate our business, for legal and marketing purposes.
+Added: Accordingly, we are, or may become, subject to numerous federal, state, local, and foreign data privacy and security laws, regulations, guidance and industry standards as well as external and internal privacy and security policies, contracts and other obligations that apply to the processing of personal data by us and on our behalf.
+Added: The legal framework for the collection, use, safeguarding, sharing, transfer and other processing of information worldwide is rapidly evolving and may remain unsettled for the foreseeable future.
+Added: Outside the United States, an increasing number of laws, regulations, and industry standards apply to data privacy and security.
+Added: For example, the European Union’s General Data Protection Regulation (GDPR) and the United Kingdom’s GDPR (UK GDPR) imposes strict obligations on the processing of personal data, including, without limitation, and personal health data.
+Added: The GDPR and UK GDPR set out extensive compliance requirements, including providing detailed disclosures about how personal data is collected and processed, demonstrating that an appropriate legal basis is in place or otherwise exists to justify data processing activities;
+Added: granting new rights for data subjects in regard to their personal data, as well as enhancing pre-existing rights (e.g., data subject access requests);
+Added: requiring the appointment of a data protection officer in certain circumstances;
+Added: mandating the appointment of representatives in the United Kingdom and/or the EEA in certain circumstances;
+Added: introducing the obligation to notify data protection regulators or supervisory authorities (and in certain cases, affected individuals) of significant data breaches;
+Added: imposing limitations on retention of personal data;
+Added: maintaining a record of data processing;
+Added: and complying with the principle of accountability and the obligation to demonstrate compliance through policies, procedures, training and audit.
+Added: The processing of sensitive personal data, such as health information, impose heightened compliance burdens under the GDPR and the UK Data Protection Act and is a topic of active interest among foreign regulators.
+Added: Moreover, the GDPR and the UK Data Protection Act increase our obligations with respect to clinical trials conducted in the EU and the UK by expanding the definition of personal data to include coded data and requiring changes to informed consent practices and more detailed notices for clinical trial participants and investigators.
+Added: Recent legal developments in Europe have created complexity and uncertainty regarding transfers of personal data from the European Economic Area, or EEA, to the United States.
+Added: On July 16, 2020, in a case known as Schrems II, the Court of Justice of the European Union, or CJEU, invalidated the EU-US Privacy Shield Framework under which personal data could be transferred from the EEA to U.S.
+Added: entities who had self-certified under the Privacy Shield scheme.
+Added: While the CJEU upheld the adequacy of the Standard Contractual Clauses (a standard form of contract approved by the European Commission as an adequate personal data transfer mechanism, and potential alternative to the Privacy Shield), it made clear that reliance on them alone may not necessarily be sufficient in all circumstances.
+Added: Use of the standard contractual clauses must now be assessed on a case-by-case basis taking into account the legal regime applicable in the destination country, in particular applicable surveillance laws and rights of individuals and additional measures and/or contractual provisions may need to be put in place.
+Added: Additionally, new Standard Contractual Clauses that repealed the Standard Contractual Clauses adopted under the Data Protection Directive have recently been adopted on June 4, 2021 by the European Commission.
+Added: We thus are still in the process of updating all our contracts entailing the transfer of personal data outside of the European Economic Area with this new Standard Contractual Clauses.
+Added: As supervisory authorities issue further guidance on personal data export mechanisms, including on the new Standard Contractual Clauses, and/or start taking enforcement action, we could suffer additional costs, complaints and/or regulatory investigations or fines, and/or if we are otherwise unable to transfer personal data between and among countries and regions in which we conduct clinical trials, it could affect our business.
+Added: While the President of the United States and the President of the European Commission announced on March 25, 2022 that they had reached an agreement in principle for a Trans-Atlantic Data Privacy Framework, which would allow personal data to flow freely and safely between the EU and participating U.S.
+Added: companies, there are some uncertainties on whether such Trans-Atlantic Data Privacy Framework would be effectively adopted and if so, by when it would be applicable.
+Added: The agreement in principle now needs to be translated into legally binding commitments, which include the adoption by the United States of a new set of rules and binding safeguards to limit access to data by U.S.
+Added: intelligence authorities and procedures to ensure effective oversight of new privacy and civil liberties standards, as well as the implementation of a new two-tier redress system to investigate and resolve complaints by European citizens on access of data by U.S.
+Added: Intelligence authorities.
+Added: Subject to the effective implementation of such commitments by the United States, the European Commission would further launch the procedure to adopt an adequacy decision, which involves a proposal from the European Commission, an opinion of the European Data Protection Board, an approval from representatives of EU countries, and the adoption of the decision by the European Commission.
+Added: Accordingly, the new Trans-Atlantic Data Privacy Framework may not be adopted in a near future and thus, the transfer of personal data from the EU to the United States still entail in-depth legal analysis and heavy paperwork requirements until then.
+Added: Relatedly, following the United Kingdom’s withdrawal from the EEA and the EU, we also have to comply with the UK-specific requirements related to data protection, including with respect to transfer of personal data outside of the UK, which increases our regulatory compliance burden.
+Added: The UK also recently updated its transfer mechanism and we will need to update all of our contracts entailing the transfer of personal data outside of the United Kingdom with this new UK-specific transfer tools.
+Added: If we cannot implement a valid compliance mechanism for cross-border data transfers, we may face increased exposure to regulatory actions, substantial fines, and injunctions against processing or transferring personal data from Europe or elsewhere.
+Added: The inability to import personal data to the United States could significantly and negatively impact our business operations, including by limiting our ability to conduct clinical trial activities in Europe and elsewhere;
+Added: limiting our ability to collaborate with parties that are subject to European and other data privacy and security laws;
+Added: or requiring us to increase our personal data processing capabilities and infrastructure in Europe and/or elsewhere at significant expense.
+Added: Additionally, in the United States, federal, state, and local governments have enacted numerous data privacy and security laws, including data breach notification laws, personal data privacy laws, and consumer protection laws.
+Added: The California Consumer Privacy Act of 2018 (CCPA) imposes obligations on businesses to which it applies.
+Added: These obligations include, but are not limited to, providing specific disclosures in privacy notices and affording California residents certain rights related to their personal data.
+Added: The CCPA allows for statutory fines for noncompliance (up to $7,500 per violation).
+Added: In addition, it is anticipated that the California Privacy Rights Act of 2020 (CPRA), effective January 1, 2023, will expand the CCPA.
+Added: For example, the CPRA establishes a new California Privacy Protection Agency to implement and enforce the CPRA, which could increase the risk of an enforcement action.
+Added: Other states have enacted data privacy laws.
+Added: For example, Virginia passed the Consumer Data Protection Act, Colorado passed the Colorado Privacy Act and Utah passed the Utah Consumer Privacy Act all three of which differ from the CPRA and become effective in 2023.
+Added: If we become subject to new data privacy laws, at the state level, the risk of enforcement action against us could increase because we may become subject to additional obligations, and the number of individuals or entities that can initiate actions against us may increase (including individuals, via a private right of action, and state actors).
+Added: In addition, data privacy and security laws have been proposed at the federal, state, and local levels in recent years, which could further complicate compliance efforts.
+Added: Our obligations related to data privacy and security are quickly changing in an increasingly stringent fashion, creating some uncertainty as to the effective future legal framework.
+Added: Additionally, these obligations may be subject to differing applications and interpretations, which may be inconsistent or in conflict among jurisdictions.
+Added: Preparing for and complying with these obligations requires us to devote significant resources (including, without limitation, financial and time-related resources).
+Added: These obligations may necessitate changes to our information technologies, systems, and practices and to those of any third parties that process personal data on our behalf.
+Added: In addition, these obligations may require us to change our business model.
+Added: Collectively, these laws may increase our compliance costs and potential liability.
+Added: Although we endeavor to comply with our published policies, other documentation, and all applicable privacy and security laws, we may at times fail to do so or may be perceived to have failed to do so.
+Added: Moreover, despite our efforts, our personnel or third parties upon whom we rely may fail to comply with such obligations, which could negatively impact our business operations and compliance posture.
+Added: For example, any failure by a third-party processor to comply with applicable law, regulations, or contractual obligations could result in adverse effects, including inability to operate our business and proceedings against us by governmental entities or others.
+Added: If we fail, or are perceived to have failed, to address or comply with obligations related to data privacy and security, we could face government enforcement actions that could include investigations, fines, penalties, audits and inspections;
+Added: additional reporting requirements and/or oversight;
+Added: temporary or permanent bans on all or some processing of personal data;
+Added: orders to destroy or not use personal data;
+Added: and imprisonment of company officials.
+Added: Further, individuals or other relevant stakeholders could sue us for our actual or perceived failure to comply with our data privacy and security obligations, including, without limitation, in class action litigation.
+Added: Any of these events could have a material adverse effect on our reputation, business, or financial condition, and could lead to a loss of actual or prospective customers, collaborators or partners;
+Added: interrupt or stop clinical trials;
+Added: result in an inability to process personal data or to operate in certain jurisdictions;
+Added: limit our ability to develop or commercialize our products;
+Added: or require us to revise or restructure our operations.
+Added: Moreover, such suits, even if we are not found liable, could be expensive and time-consuming to defend and could result in adverse publicity that could harm our business or have other material adverse effects.
+Added: Additionally, we expect that there will continue to be new proposed laws and regulations concerning data privacy and security, and we cannot yet determine the impact such future laws, regulations and standards may have on our business.
Risks Related to the Securities Markets and Ownership of our Equity Securities
8 unchanged sentences
• media coverage regarding our industry or us;
−Removed: • litigation;
+Added: • litigation arbitration, or other adverse non-judicial proceedings;
• disputes with or our inability to collect from significant customers;
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Our federal net operating losses (NOLs) generated in taxable years beginning on or prior to December 31, 2017 could expire unused.
−Removed: Under legislation enacted in 2017, informally titled the Tax Cuts and Jobs Act, as modified by the Coronavirus Aid, Relief, and Economic Security Act (CARES Act) federal NOLs incurred in taxable years beginning after December 31, 2017, may be carried forward indefinitely, but the deductibility of such federal NOLs in tax years beginning after December 31, 2020, is limited to 80% of taxable income.
−Removed: It is uncertain if and to what extent various states will conform to the Tax Cuts and Jobs Act or the CARES Act.
+Added: Under current law, federal NOLs incurred in taxable years beginning after December 31, 2017, may be carried forward indefinitely, but the deductibility of such federal NOLs in tax years beginning after December 31, 2020, is limited to 80% of taxable income.
+Added: It is uncertain if and to what extent various states will conform to federal tax laws.
In addition, under Sections 382 and 383 of the Internal Revenue Code of 1986, as amended, and corresponding provisions of state law, if a corporation undergoes an “ownership change,” which is generally defined as a greater than 50% change (by value) in its equity ownership over a three-year period, the corporation’s ability to use its pre-change NOL carryforwards and other pre-change tax attributes (such as research tax credits) to offset its post-change income or taxes may be limited.
3 unchanged sentences
In addition, at the state level, there may be periods during which the use of NOLs is suspended or otherwise limited, which could accelerate or permanently increase state taxes owed.
−Removed: For example, California imposed limits on the usability of California state net operating losses to offset taxable income in tax years beginning after 2019 and before 2023.
We have a significant number of outstanding options and unvested restricted stock units.
Future sales of these shares could adversely affect the market price of our common stock.
−Removed: As of September 30, 2021, we had outstanding options for an aggregate of approximately 10.5 million shares of common stock at a weighted average exercise price of $4.62 per share and unvested restricted stock units of approximately 0.1 million shares.
+Added: As of March 31, 2022, we had outstanding options for an aggregate of approximately 12.0 million shares of common stock at a weighted average exercise price of $4.32 per share and unvested restricted stock units of approximately 0.4 million shares.
The holders may sell many of these shares in the public markets from time to time, without limitations on the timing, amount or method of sale.
4 unchanged sentences
(i) any derivative action or proceeding brought on our behalf, (ii) any action asserting a claim of breach of a fiduciary duty owed by any of our directors or officers to our company or our stockholders, (iii) any action asserting a claim against our company arising pursuant to any provision of the Delaware General Corporation Law or our amended and restated certificate of incorporation or Bylaws, or (iv) any action asserting a claim against our company governed by the internal affairs doctrine.
−Removed: This choice of forum provision does not apply to suits brought to enforce a duty or liability created by the Securities Act of 1933, as amended, or the Exchange Act, or any other claim for which the federal courts have exclusive jurisdiction.
This choice of forum provision may limit a stockholder’s ability to bring certain claims in a judicial forum that it finds favorable for disputes with us or any of our directors, officers, other employees or stockholders, which may discourage lawsuits with respect to such claims, although our stockholders will not be deemed to have waived our compliance with federal securities laws and the rules and regulations thereunder.
+Added: While the Delaware courts have determined that such choice of forum provisions are facially valid and several state trial courts have enforced such provisions, there is no guarantee that courts of appeal will affirm the enforceability of such provisions and a stockholder may nevertheless seek to bring a claim in a venue other than that designated in the exclusive forum provision.
If a court were to find this choice of forum provision to be inapplicable or unenforceable in an action, we may incur additional costs associated with resolving such action in other jurisdictions, which could adversely affect our business and financial condition.
12 unchanged sentences
Further, existing tax laws, statutes, rules, regulations or ordinances could be interpreted, changed, modified or applied adversely to us.
−Removed: For example, the Tax Cuts and Jobs Act, enacted many significant changes to the U.S.
−Removed: Future guidance from the Internal Revenue Service and other tax authorities with respect to the Tax Cuts and Jobs Act may affect us, and certain aspects of the Tax Cuts and Jobs Act could be repealed or modified in future legislation.
−Removed: For example, the CARES Act modified certain provisions of the Tax Cuts and Jobs Act.
−Removed: In addition, it is uncertain if and to what extent various states will conform to the Tax Cuts and Jobs Act, the CARES Act, or any newly enacted federal tax legislation.
−Removed: Changes in corporate tax rates, the realization of net deferred tax assets relating to our operations, the taxation of foreign earnings, and the deductibility of expenses under the Tax Cuts and Jobs Act or future reform legislation could have a material impact on the value of our deferred tax assets, could result in significant one-time charges, and could increase our future U.S.
+Added: For example, the Biden administration and Congress have proposed various U.S.
+Added: federal tax law changes, which if enacted could have a material impact on our business, cash flows, financial condition or results of operations.
+Added: In addition, it is uncertain if and to what extent various states will conform to federal tax laws.
+Added: Future tax reform legislation could have a material impact on the value of our deferred tax assets, could result in significant one-time charges, and could increase our future U.S.
Our shares of common stock may be thinly traded, so you may be unable to sell at or near ask prices or at all.
7 unchanged sentences
In addition, the issuance of shares of our common stock upon the exercise of outstanding options or warrants may result in dilution to our stockholders.
−Removed: UNREGISTERED SALES OF EQUITY SECURITIES AND USE OF PROCEEDS
−Removed: Defaults upon Senior Securities
−Removed: MINE SAFETY DISCLOSURES
−Removed: Not applicable.
+Added: Description of Exhibits
+Added: Agreement and Plan of Merger, dated as of May 21, 2008, by and among Cody Resources, Inc., CDI Acquisition, Inc.
+Added: and ChromaDex, Inc., as amended on June 10, 2008 (incorporated by reference to, and filed as Exhibit 2.1 to the Registrant’s Current Report on Form 8-K (File No.
+Added: 333-140056) filed with the Commission on June 24, 2008) (1)
+Added: Amended and Restated Certificate of Incorporation of the Registrant (incorporated by reference to, and filed as Exhibit 3.1 to the Registrant’s Annual Report on Form 10-K (File No.
+Added: 001-37752) filed with the Commission on March 15, 2018)
+Added: Certificate of Amendment to the Amended and Restated Certificate of Incorporation of the Registrant (incorporated by reference to, and filed as Exhibit 3.1 to the Registrant’s Current Report on Form 8-K (File No.
+Added: 000-53290) filed with the Commission on April 12, 2016)
+Added: Amended and Restated Bylaws of the Registrant (incorporated by reference to, and filed as Exhibit 3.3 to the Registrant’s Annual Report on Form 10-K (File No.
+Added: 001-37752) filed with the Commission on March 15, 2022)
+Added: Form of Stock Certificate representing shares of the Registrant’s Common Stock (incorporated by reference to, and filed as Exhibit 4.1 to the Registrant’s Annual Report on Form 10-K (File No.
+Added: 000-53290) filed with the Commission on April 3, 2009)
+Added: Investor’s Rights Agreement, effective as of December 31, 2005, by and between The University of Mississippi Research Foundation and the Registrant (incorporated by reference to, and filed as Exhibit 4.1 to the Registrant’s Current Report on Form 8-K (File No.
+Added: 333-140056) filed with the Commission on June 24, 2008)
+Added: Tag-Along Agreement effective as of December 31, 2005, by and among the Registrant, Frank Louis Jaksch, Snr.
+Added: & Maria Jaksch, Trustees of the Jaksch Family Trust, Margery Germain, Lauren Germain, Emily Germain, Lucie Germain, Frank Louis Jaksch, Jr., and the University of Mississippi Research Foundation (incorporated by reference to, and filed as Exhibit 4.2 to the Registrant’s Current Report on Form 8-K (File No.
+Added: 333-140056) filed with the Commission on June 24, 2008)
+Added: Form of Stock Certificate representing shares of the Registrant’s Common Stock effective as of January 1, 2016 (incorporated by reference to, and filed as Exhibit 4.4 to the Registrant’s Annual Report on Form 10-K (File No.
+Added: 001-37752) filed with the Commission on March 17, 2016)
+Added: Form of Stock Certificate representing shares of the Registrant’s Common Stock effective as of December 10, 2018 (incorporated by reference to, and filed as Exhibit 4.5 to the Registrant’s Annual Report on Form 10-K (File No.
+Added: 001-37752) filed with the Commission on March 7, 2019)
+Added: Registration Rights Agreement, dated as of May 9, 2019, by and among the Registrant and the parties thereto (incorporated by reference to Exhibit 99.2 to the Registrant’s Current Report on Form 8-K filed with the SEC on May 10, 2019)
+Added: Registration Rights Agreement, dated as of August 15, 2019, by and among the Registrant and the parties thereto (incorporated by reference to Exhibit 99.1 to the Registrant’s Current Report on Form 8-K filed with the SEC on August 15, 2019)
+Added: Registration Rights Agreement, dated as of April 27, 2020, by and among the Registrant and the parties thereto (incorporated by reference to Exhibit 99.2 to the Registrant’s Current Report on Form 8-K filed with the SEC on April 29, 2020)
+Added: Registration Rights Agreement, dated February 20, 2021, by and among the Company and the Purchaser (incorporated by reference to Exhibit 99.2 to the Registrant’s Current Report on Form 8-K filed with the SEC on February 22, 2021)
+Added: Second Amendment to the Amended and Restated Exclusive License Agreement, effective as of January 1, 2022, between Dartmouth College and ChromaDex, Inc.
+Added: First Amendment to the Amended and Restated Exclusive License Agreement, effective as of December 29, 2020, between Dartmouth College and ChromaDex, Inc.
+Added: Side letter agreement to the Amended and Restated Exclusive License Agreement, effective as of March 13, 2019, between Dartmouth College and ChromaDex, Inc.
+Added: Restated and Amended Exclusive License Agreement, effective as of March 13, 2017, between Dartmouth College and ChromaDex, Inc.
+Added: First Amendment to the Joint Ownership Management Agreement, effective March 9, 2022, between Queen’s University of Belfast and ChromaDex, Inc.**❖
+Added: Joint Ownership Management Agreement, effective October 9, 2015, between Queen’s University of Belfast and ChromaDex, Inc.**❖
+Added: Description of Exhibits
+Added: Transition and Separation Agreement, effective July 8, 2021, between Lisa Harrington and ChromaDex, Inc.
+Added: Certification of the Chief Executive Officer pursuant to Rule 13a-14(A) of the Securities Exchange Act of 1934, as amended❖
+Added: Certification of the Chief Financial Officer pursuant to Rule 13a-14(A) of the Securities Exchange Act of 1934, as amended❖
+Added: Certification pursuant to 18 U.S.C.
+Added: Section 1350 (as adopted pursuant to Section 906 of the Sarbanes−Oxley Act of 2002)❖
+Added: 101.INS Inline XBRL Instance Document- the instance document does not appear in the Interactive Data File because its XBRL tags are embedded within the Inline XBRL document
+Added: 101.SCH Inline XBRL Taxonomy Extension Schema Document
+Added: 101.CAL Inline XBRL Taxonomy Extension Calculation Linkbase Document
+Added: 101.DEF Inline XBRL Taxonomy Extension Definition Linkbase Document
+Added: 101.LAB Inline XBRL Taxonomy Extension Label Linkbase Document
+Added: 101.PRE Inline XBRL Taxonomy Extension Presentation Linkbase Document
+Added: 104 104 Cover Page Interactive Data File (formatted as Inline XBRL and contained in Exhibit 101)
+Added: v Filed herewith.
+Added: (1) Plan and related Forms were assumed by ChromaDex Corporation pursuant to Agreement and Plan of Merger, dated as of May 21, 2008, among ChromaDex Corporation (formerly Cody Resources, Inc.), CDI Acquisition, Inc.
+Added: and ChromaDex, Inc.
+Added: (2) Schedules have been omitted pursuant to Item 601(a)(5) of Regulation S-K.
+Added: ChromaDex Corporation undertakes to furnish supplemental copies of any of the omitted schedules upon request by the Securities and Exchange Commission;
+Added: provided, however, that ChromaDex Corporation may request confidential treatment pursuant to Rule 24b-2 of the Securities Exchange Act of 1934, as amended, for any schedule so furnished.
+Added: ** Certain portions of this exhibit (indicated by asterisks) have been excluded pursuant to Item 601(b)(10) of Regulation S-K because they are both not material and are the type that the Registrant treats as private or confidential.
+Added: Pursuant to the requirements of the Securities Exchange Act of 1934, the Registrant has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized.
+Added: CHROMADEX CORPORATION
+Added: May 12, 2022 /s/ KEVIN M.
+Added: Chief Financial Officer
+Added: (principal financial and accounting officer and duly authorized on behalf of the registrant)
Compared sentence by sentence after normalising whitespace, quotation marks, case and digits, so re-formatting and restated figures do not read as changed language. Wording changes appear as one removal and one addition. The current filing and the prior one are authoritative.