Item 1. Business
Company Overview
We, through our wholly owned subsidiary Skinvisible Pharmaceuticals Inc.,
are a pharmaceutical research and development (“R&D”) company that has developed and patented an innovative polymer delivery
system, Invisicare® and formulated over forty topical skin products, which we out-license globally. We were incorporated in 1998,
and target an estimated $80 billion global skincare and dermatology market and a $30 billion global over-the-counter market as well as
other healthcare / medical and consumer goods markets.
With the research and development complete on forty products and numerous
patents issued (technology and product patents), we are ready to monetize our investment. Our business model will continue to be to out-license
our patented prescription and over-the-counter (“OTC”) products featuring Invisicare to established manufacturers and marketers
of brands internationally and to maximize profits from the products we have already out-licensed.
The opportunity for us to license our products continues to be a viable
model as the need for pharmaceutical companies to access external R&D companies for new products due to their own down-sizing or elimination
of internal R&D departments. The demand for our products is enhanced due to the granting of key US and international patents and the
completed development of a number of unique products.
Our Flagship Product
Pivotal to our success is our patented polymer delivery system technology
Invisicare. Invisicare is a patented polymer delivery system that enhances the delivery of active ingredients for topically applied skin
care products. Its patented technology has a unique formula and process for combining active ingredients with a delivery system that extends
the duration of time the product remains on the skin and active.
Invisicare is specifically formulated to carry water insoluble active
and certain cationic active ingredients in water-based products without the use of alcohol, silicones, waxes, or other organic solvents.
Products utilizing Invisicare have the proven ability to bond active ingredients to the skin for up to four hours and longer. They are
non-occlusive and allow normal skin respiration and perspiration while moisturizing and protecting against exposure from a wide variety
of environmental irritants.
When topically applied, these formulated products adhere to the skin's
outer layers, forming a protective bond, resisting wash-off, and delivering targeted levels of therapeutic or cosmetic skincare agents
to the skin. They allow enhanced delivery performance for a variety of skincare agents resulting in improved efficacy, longer duration
of action, reduced irritation and lower dosage of active agent required. The "invisible" polymer compositions wear off as part
of the natural exfoliation process of the skin's outer layer cells.
The advantage of products formulated with Invisicare is (1) Invisicare’s
ability to bind active ingredients (the drug) to the skin, forming a protective bond on the skin, for extended periods of time; (2) Invisicare
can deliver targeted levels (high or low) of therapeutic or cosmetic ingredients to the skin in a controlled release; (3) Invisicare can
help to reduce the irritation of some active ingredients due to how it controls the slower release of that active ingredient; and (4)
Invisicare science proves that it provides a protective skin barrier which helps retain the natural moisture content of the skin, while
still allowing it to breathe. These benefits present an excellent opportunity for clear scientific advantages and marketing messages which
resonate with physicians and consumers.
We have positioned ourselves in the $80 billion
worldwide prescription and over-the-counter dermatology and skincare market. We generate revenue by:
- LICENSING:
We develop topical prescription and over-the-counter products enhanced with Invisicare to license to pharmaceutical and consumer goods
companies around the world for an upfront fee and ongoing royalties;
- CO-DEVELOPMENT: We assist pharmaceutical
clients in the early development of the most optimal formulation, which they then take forward into clinical testing;
- LIFE CYCLE MANAGEMENT: We provide cost-effective
solutions to global pharmaceutical companies by reformulating their products coming off patent with a new Invisicare patent and new product
benefits and line extensions. Pharmaceutical companies are under a lot of pressure to develop innovative strategies to counteract the
revenue loss from their drugs coming off patent.
License Agreement with Quoin
On October 17, 2019, we entered an Exclusive License
Agreement with Quoin Pharmaceuticals, Inc., a Delaware corporation (“Quoin”) pursuant to which we granted to Quoin a license
to certain patents for the development of products for commercial sale. In exchange for the license, Quoin agreed to pay to us a license
fee of $1,000,000 (the “License Fee”) and a single digit royalty interest of all net sales on the licensed products subject
to adjustment in certain situations. The agreement also requires that Quoin make certain milestone payments to us upon achieving regulatory
approval milestones for certain drug products.
The agreement was subject to termination,
if among other things, 50% of the license fee is not paid by December 31, 2019 and if the full License Fee is not paid by March 31, 2020.
No payments were made by Quoin and the agreement was terminated. Both Parties subsequently determined that they continue to see the value
in a partnership and therefore on May 8, 2020 and again on July 31, 2020 the companies agreed to extend the Exclusive License Agreement
under the same terms to expire on December 31, 2020, and on January 27, 2021 the companies agreed to revise the milestone payments due
under the agreement and to extend the agreement indefinitely.
On June 14, 2021, the Company entered into an
amendment to change the terms of the license Fee as shown below.
As partial consideration for the rights
conveyed by Skinvisible under this Agreement, Licensee agrees to pay to Skinvisible a one-time, non-refundable, non-creditable license
issue fee of one million USD dollars (USD $1,000,000) (''License Fee''). To date, Licensee has paid one million US dollars (USD $1,000,000).
Additionally, the milestones in the initial agreement
were changed as shown below:
(i) Successful
completion of Phase 2 testing: $0
(ii) Successful
completion of Phase 3 testing: $0
(iii) Regulatory
approval in either the US or EU, whichever happens first: $5,000,000
On June 6, 2022 we announced
that Quoin has received U.S. FDA acceptance of its Investigational New Drug (IND) application for its licensed formulation which uses
our Invisicare proprietary drug delivery technology. The topical formulation "QRX003" was developed to treat Nethertons Syndrome,
a debilitating hereditary disorder that affects the skin, hair and the immune system. There currently is no cure or approved treatment
for Netherton Syndrome.
With the IND approved, the
clinical trial is underway. We look forward to assisting Quoin in their success and potential FDA approval as well as potentially bringing
a treatment to patients suffering from Nethertons Syndrome.
Quoin is responsible for
obtaining all FDA and other regulatory body approvals necessary to market the products in the US and other countries. Upon the successful
completion of various clinical and regulatory milestones, Skinvisible is entitled to receive a milestone payment of $5 million and ongoing
royalties from sales.
License Agreement with Ovation Science
On February 3, 2020, we entered into a License
Agreement with Ovation Science Inc. pursuant to which Skinvisible granted to Ovation Science Inc. a license for the manufacture and distribution
rights to its hand sanitizer product, DermSafe. In exchange for the license, Ovation Science Inc. agreed to pay to Skinvisible a royalty
percentage on all net sales on the licensed products subject to adjustment in certain situations plus a license fee payable in year 3
of the agreement if it chooses to continue the license.
On June 10, 2020, Ovation Science paid us the
fee otherwise due in year 3 and in exchange we extended the term of Ovation Science’s license to 6-years and granted Ovation additional
rights to its hand sanitizer products and assigned Canadian Identification Numbers 02310589 and 02355558, all DermSafe Trademarks, DermSafe
clinical data and the right to patent DermSafe where not currently patented. In exchange for these rights, Ovation Science paid a $100,000
license fee. We completed the required assignments during the year ending December 31, 2020 and recognized $100,000 in revenue.
Competition
Market research indicates there is reasonably limited direct competition
for Invisicare and patented products in terms of performance capabilities for topically administered skin products. Many companies are
seeking unique delivery systems to enhance their portfolio and purchasing companies that have delivery technology.
Government Regulation
Cosmetic and Skin Care Regulation
Depending upon product claims and formulation, skin care products may be
regulated as cosmetics, drugs, devices, or combination cosmetics and drugs. The FDA has authority to regulate cosmetics marketed in the
United States under the FDCA and the Fair Packaging and Labeling Act (“FPLA”) and implementing regulations. The Federal Trade
Commission (the “FTC”) regulates the advertising of cosmetics under the FTCA.
The FDCA prohibits the marketing of adulterated and misbranded cosmetics.
Cosmetic ingredients must also comply with the FDA’s ingredient, quality, and labeling requirements and the FTC’s requirements
pertaining to truthful and non-misleading advertising. Cosmetic products and ingredients, with the exception of color additives, are not
required to have FDA premarket approval. Manufacturers of cosmetics are also not required to register their establishments, file data
on ingredients, or report cosmetic-related injuries to the FDA.
We will be responsible for substantiating the safety and product claims
of the cosmetic products and ingredients before marketing. The FDA or FTC may disagree with our characterization of one or more of the
skin care products as a cosmetic or the product claims. This could result in a variety of enforcement actions which could require the
reformulation or relabeling of our products, the submission of information in support of the product claims or the safety and effectiveness
of our products, or more punitive action, all of which could have a material adverse effect on our business. If the FDA determines we
have failed to comply with applicable requirements under the FDCA or FPLA, it can impose a variety of enforcement actions from public
warning letters, injunctions, consent decrees, and civil penalties to seizure of our products, total or partial shutdown of our production,
and criminal prosecutions. If any of these events were to occur, it could materially adversely affect us. If the FTC determines we have
failed to substantiate our claims, it can pursue a variety of actions including disgorgement of profits, injunction from further violative
conduct, and consent decrees.
Domestic State and Local Government Regulation
Some states and local governments in the United States regulate the labeling,
operation, sale, and distribution of our skin care products. To the extent additional state or local laws apply, we intend to comply with
them.
Foreign Government Regulation
In general, we will need to comply with the government regulations of each
individual country in which our products are to be distributed and sold. These regulations vary in complexity and can be as stringent,
and on occasion even more stringent, than FDA regulations in the United States. The level of complexity and stringency is not always precisely
understood today for each country, creating greater uncertainty for the international regulatory process. Furthermore, government regulations
can change with little to no notice and may result in up-regulation of our product(s), thereby creating a greater regulatory burden for
us. We have not yet thoroughly explored the applicable laws and regulations that we will need to comply with in foreign jurisdictions.
As a result it is possible that we may not be permitted to sell our products in foreign markets or expand our business into one or more
foreign jurisdictions.
Environmental Laws
We are not subject to any significant or material environmental regulation
in the normal operation of our business.
Employees
Currently, we have two employees, including our CEO Terry Howlett.
Subsidiaries
We conduct our operations through our wholly-owned subsidiary, Skinvisible
Pharmaceuticals, Inc.
Item 1A. Risk Factors
Risk Factors Associated with Covid 19
The extent to which the coronavirus (“COVID-19”) outbreak
impacts our business, results of operations and financial condition will depend on future developments, which cannot be predicted.
The COVID-19 pandemic has caused us to modify our business practices (including
employee travel, employee work locations, and cancellation of physical participation in meetings, events and conferences), and we may
take further actions as may be required by government authorities or that we determine are in the best interests of our employees, customers
and business partners. There is no certainty that such measures will be sufficient to mitigate the risks posed by the virus or otherwise
be satisfactory to government authorities.
The extent to which COVID-19 impacts our business, results of operations
and financial condition will depend on future developments, which are uncertain and cannot be predicted, including, but not limited to:
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the duration and scope of the pandemic; |
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governmental, business and individual actions taken in response to the pandemic and the impact of those actions on global economic activity; |
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the actions taken in response to economic disruption; |
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the impact of business disruptions; |
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the increase in business failures that we may utilize as industry partners and the customers we serve; |
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uncertainty as to the impact or staff availability during and post the pandemic; and |
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our ability to provide our services, including as a result of our employees or our customers and suppliers working remotely and/or closures of offices and facilities. |
Even after the coronavirus outbreak has subsided, we may continue to experience
materially adverse impacts to our business as a result of its global economic impact, including any recession that has occurred or may
occur in the future.
Risks Related to Our Financial Condition and our Business
We have outstanding secured and other debt that has matured and we
have not paid off, which could negatively affect our ability to continue as a going concern.
We
expect to experience high debt payments in the future as a result of our outstanding secured and unsecured liabilities. During the year
ended December 31, 2021, we entered to settlement agreements to settle various notes. As part of the settlement the principal balance
of the notes were settled for cash and all interest due through the date of settlement was forgiven. As of December 31, 2021, the Company
has recorded a gain on settlement of the debt of $109,688 associated with the settlement of $298,400 of principal. As of December 31,
2022, $443,600 of the outstanding secured notes payable are past due and in default and have been classified as current notes payable.
We also have $40,000 in
outstanding unsecured notes that are past due. If we are unable to generate sufficient revenues and/or additional financing to service
this debt, there is a risk the lenders will call the notes, secure our assets, as to those applicable secured notes, and demand payment.
If this happens, we could go out of business.
Our investors may lose their entire investment because our financial
status creates a doubt whether we will continue as a going concern.
We do not have sufficient cash nor
do we have a significant source of revenues to cover our operational costs and allow us to continue as a going concern. The
Company anticipates generating revenues through the licensing of its core products and if that is not sufficient we may seek to raise
additional operating capital to implement our business plan in an offering of our common stock or debt. Our company's plan
specifies a minimum amount of $500,000 in additional operating capital to operate for the next twelve months. However, there can be no
assurance that the revenues generated or that such an offering will be successful. You may lose your entire investment
Our failure to raise additional
capital or generate cash flows necessary to expand our operations could reduce our ability to compete successfully and adversely affect
our results of operations.
We need to raise additional funds
to achieve our future strategic objectives, and we may not be able to obtain additional debt or equity financing on favorable terms, if
at all. If we engage in debt financing, we may be required to accept terms that restrict our ability to incur additional indebtedness,
force us to maintain specified liquidity or other ratios or restrict our ability to pay dividends or make acquisitions. If we need additional
capital and cannot raise it on acceptable terms, we may not be able to, among other things:
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launch, develop and enhance
our existing products;
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continue to expand our product
base, sales and/or marketing efforts;
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hire, train and retain employees;
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respond to competitive pressures
or unanticipated working capital requirements.
Our inability to do any of the foregoing
could reduce our ability to compete successfully and adversely affect our results of operations.
If we are unable to generate revenues by implementing our business
plan, you will lose your entire investment in our company.
We have a history of losses from inception and we had an accumulated deficit
as of December 31, 2022 of $36,998,048. We have not been able to generate sufficient revenues from licensees, from the sale of our own
products or otherwise to cover our expenses. If we are unsuccessful in generating revenues, you could lose your entire investment.
If our products or products that are licensed by our licensees are
not deemed desirable and suitable for purchase and we cannot establish a customer base, we may not be able to generate sufficient revenues,
which would result in a failure of the business and a loss of any investment one makes in our company.
The acceptance of our products is critically important to our success.
We cannot be certain that the products that we will be offering will be appealing and as a result there may not be any demand for these
products and our sales could be limited and we may never realize any significant revenues. In addition, there are no assurances that if
we alter or change the products we offer in the future that the demand for these new products will develop and this could adversely affect
our business and any possible revenues.
If demand for the products that we offer or products that are licensed
by our licensees slows, then our business would be materially affected.
Demand for our products and products of our licensees, depends on many
factors, including:
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the economy, and in periods of rapidly declining economic conditions, customers may defer luxury purchases or may choose alternate products; |
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the competitive environment in the skin care sector or sectors in which products are introduced may force us to reduce prices below our desired pricing level or increase promotional spending; |
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our ability to anticipate changes in consumer preferences and to meet customers’ needs for skin care products in a timely cost-effective manner; |
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our ability to maintain efficient, timely and cost-effective production and delivery of the products and services; and, |
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our ability to identify and respond successfully to emerging trends in the skin care and personal care industries. |
For the long term, demand for product offerings may be affected by:
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the ability to establish, maintain and eventually grow market share in a competitive environment; |
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our ability to deliver our products in the markets we intend to service, changes in government regulations, currency fluctuations, natural disasters, pandemics and other factors beyond our control may increase the cost of items we purchase, create communication issues or render product delivery difficult which could have a material adverse effect on our sales and profitability; and |
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restrictions on access to North American markets and supplies. |
All of these factors could result in immediate and longer term declines
in the demand for products that we offer as well as licensed products, which could adversely affect our sales, cash flows and overall
financial condition.
Because we are new in the marketplace, we may not be able to compete
effectively and increase market share.
Our current and potential competitors may have longer operating histories,
significantly greater resources and name recognition, and a larger base of customers than we have. Our competitors may also be able to
adopt more aggressive pricing policies and devote greater resources to the development, marketing and sale of their products and services
than we can. To be competitive, we must continue to invest significant resources in sales and marketing. We may not have sufficient resources
to make these investments or to develop the technological advances necessary to be competitive, which in turn will cause our business
to suffer and restrict our profitability potential.
Because we rely on third parties to manufacture our products, we
are subject to factors outside of our control to meet our standards or timelines.
Our products are manufactured by three third-party manufacturing companies
on a purchase order basis. No contractual arrangement are currently in place, except for standard confidentiality agreements. We are dependent
on the timeliness and effectiveness of our third-part manufacturers’ efforts.
Failure or lack of reliability in the manufacture of our products is likely
to result in loss of business. Among other risks:
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Our products may fail to provide the expected results; |
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We may experience limited availability of quality ingredients for manufacturing; |
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We may experience poor quality manufacturing; |
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Our products may have new competition from other companies attempting to duplicate our formulas; and |
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Our customers could experience results different from our test results. |
Like other retailers, distributors and manufacturers of skin care
and personal care products, we face an inherent risk of exposure to product liability claims in the event that the use of the products
that we sell results in injury.
We may be subjected to various product liability claims, including claims
that the products we sell contain contaminants, are improperly labeled or include inadequate instructions as to use or inadequate warnings
concerning side effects and interactions with other substances. In addition, we may be forced to defend lawsuits. We cannot predict whether
product liability claims will be brought against us in the future or the effect of any resulting adverse publicity on the business. Moreover,
we may not have adequate resources in the event of a successful claim against us. The successful assertion of product liability claim
against us could result in potentially significant monetary damages. In addition, interactions of the products with other similar products,
prescription medicines and over-the-counter drugs have not been fully explored.
We may also be exposed to claims relating to product advertising or product
quality. People may purchase our products expecting certain physical results, unique to skin care and personal care products. If they
do not perceive expected results to occur, certain individuals or groups of individuals may seek monetary retribution.
If our products become contaminated, our business could be
seriously harmed.
We have adopted various quality, environmental, health and safety standards.
However, our products may still not meet these standards or could otherwise become contaminated. A failure to meet these standards or
contamination could occur in our operations or those of our bottlers, manufacturers, distributors or suppliers. Such a failure or contamination
could result in expensive production interruptions, recalls and liability claims. Moreover, negative publicity could be generated even
from false, unfounded or nominal liability claims or limited recalls. Any of these failures or occurrences could negatively affect our
business and financial performance.
Our business may be adversely affected by unfavorable publicity within
the skin care markets.
Management believes that the skin care market and personal care markets
are significantly affected by national media attention. As with any retail provider, future scientific research or publicity may not be
favorable to the industry or to any particular product, and may not be consistent with earlier favorable research or publicity. Because
of our dependence on consumers’ perceptions, adverse publicity associated with illness or other adverse effects resulting from the
use of our products or any similar products distributed by other companies and future reports of research that are perceived as less favorable
or that question earlier research, could have a material adverse effect on our business, financial condition and results of operations.
We are highly dependent upon consumers’ perceptions of the safety and quality of the products as well as similar products distributed
by other companies. Thus, the mere publication of reports asserting that skin care or personal care products may be harmful or questioning
their efficacy could have a material adverse effect on our business, financial condition and results of operations, regardless of whether
such reports are scientifically supported or whether the claimed harmful effects would be present at the dosages recommended for such
products.
As we conduct international business transactions, we will be exposed
to local business risks in different countries, which could have a material adverse effect on our financial condition or results of operations.
We promote and sell our products internationally and our licensees do the
same. International operations will be subject to risks inherent in doing business in foreign countries, including, but not necessarily
limited to:
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new and different legal and regulatory requirements in local jurisdictions; |
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potentially adverse tax consequences, including imposition or increase of taxes on transactions or withholding and other taxes on remittances and other payments by subsidiaries; |
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risk of nationalization of private enterprises by foreign governments; |
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legal restrictions on doing business in or with certain nations, certain parties and/or certain products; and, |
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local economic, political and social conditions, including the possibility of hyperinflationary conditions and political instability. |
We may not be successful in developing and implementing policies and strategies
to address the foregoing factors in a timely and effective manner in the locations where we will do business. Consequently, the occurrence
of one or more of the foregoing factors could have a material adverse effect on our base operations and upon our financial condition and
results of operations.
Since our products will be available over the Internet in foreign countries
and we plan to have customers residing in foreign countries, foreign jurisdictions may require us to qualify to do business in their country.
We will be required to comply with certain laws and regulations of each country in which we conduct business, including laws and regulations
currently in place or which may be enacted related to Internet services available to the residents of each country from online sites located
elsewhere.
Because of the nature of our products, we may be subject to government
regulations or laws that increase our costs of operations or decrease our ability to generate income.
Any failure by us, or by any third party that may manufacture or market
our products, to comply with the law, including statutes and regulations administered by the FDA or other U.S. or foreign regulatory authorities,
could result in, among other things, warning letters, fines and other civil penalties, suspension of regulatory approvals and the resulting
requirement that we suspend sales of our products, refusal to approve pending applications or supplements to approved applications, export
or import restrictions, interruption of production, operating restrictions, closure of the facilities used by us or third parties to manufacture
our product candidates, injunctions or criminal prosecution. Any of the foregoing actions could have a material adverse effect on our
business.
Our commercial success depends significantly on our ability to develop
and commercialize our potential products without infringing the intellectual property rights of third parties.
Our commercial success will depend, in part, on operating our business
without infringing the patents or proprietary rights of third parties. Third parties that believe we are infringing on their rights could
bring actions against us claiming damages and seeking to enjoin the development, marketing and distribution of our products. If we become
involved in any litigation, it could consume a substantial portion of our resources, regardless of the outcome of the litigation. If any
of these actions are successful, we could be required to pay damages and/or to obtain a license to continue to develop or market our products,
in which case we may be required to pay substantial royalties. However, any such license may not be available on terms acceptable to us
or at all. Ultimately, we could be prevented from commercializing a product or forced to cease some aspect of our business operations
as a result of patent infringement claims, which would harm our business.
The implementation of our business plan relies on our ability to
manage growth. If we are not able to manage the growth, our business plan may not be successfully implemented.
We expect to expand our operations by increasing our sales and marketing
efforts, research and development activities, and escalating our services. The anticipated growth could place a significant strain on
our management, and operational and financial resources. Effective management of the anticipated growth shall require expanding our management
and financial controls, hiring additional appropriate personnel as required, and developing additional expertise by existing management
personnel. However, there can be no assurances that these or other measures we may implement shall effectively increase our capabilities
to manage such anticipated growth or to do so in a timely and cost-effective manner. Moreover, management of growth is especially challenging
for a company with a short revenue generating history and limited financial resources, and the failure to effectively manage growth could
have a material adverse effect on our operations.
Our success depends on continuing to hire and retain qualified personnel,
including our director and officers and our technical personnel. If we are not successful in attracting and retaining these personnel,
our business will suffer.
Our success depends substantially on the performance
of our management team and key personnel. Currently, we have three employees, including our CEO Terry Howlett. Due to the specialized
technical nature of our business, we are particularly dependent on our technical personnel. Our future success will depend on our ability
to attract, integrate, motivate and retain qualified technical, sales, operations, and managerial personnel, as well as our ability to
successfully implement a plan for management succession. Competition for qualified personnel in our business areas is intense, and we
may not be able to continue to attract and retain key personnel. In addition, if we lose the services of any of our management team or
key personnel and are not able to find suitable replacements in a timely manner, our business could be disrupted and we may incur increased
operating expenses.
If
we are unable to attract new distributors and customers, or if our existing
distributors and customers do not purchase additional products, the growth of our business
and cash flows will be adversely affected.
To increase
our revenues and cash flows, we must regularly add distributors and customers and sell additional
products to our existing distributors and customers. If we are unable to sell our products
to customers that have been referred to us, unable to generate sufficient sales leads through our marketing programs, or if our existing
or new distributors and customers do not perceive our products to be of sufficiently high
value and quality, we may not be able to increase sales and our operating results would be adversely affected. In addition, if we fail
to sell new products to existing distributors and customers or new distributors and
customers, our operating results will suffer, and our revenue growth, cash flows and profitability
may be materially and adversely affected.
Key management personnel may leave us, which could adversely
affect our ability to continue operations.
We are entirely dependent on the efforts of our management because of the
time and effort that they devote to us. They are in charge of overseeing all development strategies, supervising any/all future personnel,
and the implementation of our business plan. Their loss, or other key personnel in the future, could have a material adverse effect on
our business, financial condition and results of operations.
Risks Related to Our Securities
If a market for our common stock does not develop, shareholders may
be unable to sell their shares.
Our common stock is quoted under the symbol “SKVI” on the OTCQB
operated by OTC Markets Group, Inc, an electronic inter-dealer quotation medium for equity securities. We do not currently have an active
trading market. There can be no assurance that an active and liquid trading market will develop or, if developed, that it will be sustained.
Our securities are very thinly traded. Accordingly, it may be difficult
to sell shares of our common stock without significantly depressing the value of the stock. Unless we are successful in developing continued
investor interest in our stock, sales of our stock could continue to result in major fluctuations in the price of the stock.
Our common stock price may be volatile and could fluctuate widely
in price, which could result in substantial losses for investors.
The market price of our common stock is likely to be highly volatile and
could fluctuate widely in price in response to various factors, many of which are beyond our control, including:
- technological innovations or new products and services by us or our competitors;
- government regulation of our products and services;
- the establishment of partnerships with other technology companies;
- intellectual property disputes;
- additions or departures of key personnel;
- sales of our common stock
- our ability to integrate operations, technology, products and services;
- our ability to execute our business plan;
- operating results below expectations;
- loss of any strategic relationship;
- industry developments;
- economic and other external factors; and
- period to period fluctuations in our financial results.
Because we have nominal revenues to date, you should consider any one of
these factors to be material. Our stock price may fluctuate widely as a result of any of the above.
In addition, the securities markets have from time to time experienced
significant price and volume fluctuations that are unrelated to the operating performance of particular companies. These market fluctuations
may also materially and adversely affect the market price of our common stock.
We have not paid cash dividends in the past and do not expect to
pay cash dividends in the future on our common stock. Any return on investment may be limited to the value of our common stock.
We have never paid cash dividends on our common stock and do not anticipate
paying cash dividends in the foreseeable future. The payment of cash dividends on our common stock will depend on earnings, financial
condition and other business and economic factors at such time as the board of directors may consider relevant. If we do not pay cash
dividends, our common stock may be less valuable because a return on your investment will only occur if its stock price appreciates.
As a new investor, you will experience substantial dilution
as a result of future equity issuances.
In the event we are required to raise additional capital it may do so by
selling additional shares of common stock thereby diluting the shares and ownership interests of existing shareholders.
Because we are subject to the “Penny Stock” rules, the
level of trading activity in our stock may be reduced.
The Securities and Exchange Commission has adopted regulations which generally
define "penny stock" to be any listed, trading equity security that has a market price less than $5.00 per share or an exercise
price of less than $5.00 per share, subject to certain exemptions. The penny stock rules require a broker-dealer, prior to a transaction
in a penny stock not otherwise exempt from the rules, to deliver a standardized risk disclosure document that provides information about
penny stocks and the risks in the penny stock market. The broker-dealer must also provide the customer with current bid and offer quotations
for the penny stock, the compensation of the broker-dealer and its salesperson in the transaction, and monthly account statements showing
the market value of each penny stock held in the customer’s account. In addition, the penny stock rules generally require that prior
to a transaction in a penny stock, the broker-dealer make a special written determination that the penny stock is a suitable investment
for the purchaser and receive the purchaser’s written agreement to the transaction. These disclosure requirements may have the effect
of reducing the level of trading activity in the secondary market for a stock that becomes subject to the penny stock rules which may
increase the difficulty Purchasers may experience in attempting to liquidate such securities.
Provisions in the Nevada Revised Statutes and our Bylaws could make
it very difficult for an investor to bring any legal actions against our directors or officers for violations of their fiduciary duties
or could require us to pay any amounts incurred by our directors or officers in any such actions.
Members of our board of directors and our officers will have no liability
for breaches of their fiduciary duty of care as a director or officer, except in limited circumstances, pursuant to provisions in the
Nevada Revised Statutes and our Bylaws as authorized by the Nevada Revised Statutes. Specifically, Section 78.138 of the Nevada Revised
Statutes provides that a director or officer is not individually liable to the company or its shareholders or creditors for any damages
as a result of any act or failure to act in his or her capacity as a director or officer unless it is proven that (1) the director’s
or officer’s act or failure to act constituted a breach of his or her fiduciary duties as a director or officer and (2) his or her
breach of those duties involved intentional misconduct, fraud or a knowing violation of law. This provision is intended to afford directors
and officers protection against and to limit their potential liability for monetary damages resulting from suits alleging a breach of
the duty of care by a director or officer. Accordingly, you may be unable to prevail in a legal action against our directors or officers
even if they have breached their fiduciary duty of care. In addition, our Bylaws allow us to indemnify our directors and officers from
and against any and all costs, charges and expenses resulting from their acting in such capacities with us. This means that if you were
able to enforce an action against our directors or officers, in all likelihood, we would be required to pay any expenses they incurred
in defending the lawsuit and any judgment or settlement they otherwise would be required to pay. Accordingly, our indemnification obligations
could divert needed financial resources and may adversely affect our business, financial condition, results of operations and cash flows,
and adversely affect prevailing market prices for our common stock.