Leading the way in legal advice for this fast-growing area
The global market for cannabis, hemp and CBD products continues to grow and evolve fast. We re recognized as a trailblazer in this field. Our clients benefit from multifaceted, multidisciplinary, international legal services across regulatory, transactional, and litigation matters an approach that balances risk mitigation with commercial success.
While marijuana remains a controlled substance, cannabis-related business proliferates. The global legal marijuana market is valued at USD13.2 billion (2021) and will have an annual growth rate of 25.5% to 2030. For hemp and CBD products, the figures are USD4.9 billion with growth of 21.3%.
In this fast-growing market, we re a pioneer and a thought leader, with multiple legal directory rankings.
We bring commercial insight combined with strategic advice across the cannabis, hemp and CBD supply chain: product development, licensing, distribution, sales, marketing and advertising, and everything in between. Our experience covers business-critical areas such as regulatory compliance, mergers and acquisitions, intellectual property, class action litigation, and corporate counsel.
We bring commercial insight combined with strategic advice across the cannabis, hemp and CBD supply chain.
New players continue to enter this marketplace and the industry is ever-evolving. National, regional and local regulatory landscapes are both complex and dynamic. And the scientific knowledge base is still relatively limited. Factors like these make it complicated to assemble the right team and access the mix of legal services that are required. Many firms offering capabilities in only a sub-set of your needs and, only then, in a limited geographical region. We are different.
Leading the way in legal advice for this fast-growing area
The global market for cannabis, hemp and CBD products continues to grow and evolve fast. We’re recognized as a trailblazer in this field. Our clients benefit from multifaceted, multidisciplinary, international legal services across regulatory, transactional, and litigation matters – an approach that balances risk mitigation with commercial success.
While marijuana remains a controlled substance, cannabis-related business proliferates. The global legal marijuana market is valued at USD13.2 billion (2021) and will have an annual growth rate of 25.5% to 2030. For hemp and CBD products, the figures are USD4.9 billion with growth of 21.3%.
In this fast-growing market, we’re a pioneer and a thought leader, with multiple legal directory rankings.
We bring commercial insight combined with strategic advice across the cannabis, hemp and CBD supply chain: product development, licensing, distribution, sales, marketing and advertising, and everything in between. Our experience covers business-critical areas such as regulatory compliance, mergers and acquisitions, intellectual property, class action litigation, and corporate counsel.
“We bring commercial insight combined with strategic advice across the cannabis, hemp and CBD supply chain.”
New players continue to enter this marketplace and the industry is ever-evolving. National, regional and local regulatory landscapes are both complex and dynamic. And the scientific knowledge base is still relatively limited. Factors like these make it complicated to assemble the right team and access the mix of legal services that are required. Many firms offering capabilities in only a sub-set of your needs and, only then, in a limited geographical region. We are different.
Our sector specific insights, local market experience, and global presence allow us to address diverse client requirements in this complex area, with a full-service approach and continuity across borders. We advise start-ups, SMEs and large multinationals, including marquee clients, with creative strategies and joined-up legal services.
Our multifaceted, interdisciplinary approach means we can provide a one-stop-shop for the different regulatory, transactional, and litigation matters you may face. We support diverse activities and client needs, including food and beverages, dietary supplements, drugs, devices, tobacco, private equity, and ancillary cannabis service providers.
Acreage Holdings on its USD428 million financing and reverse takeover and CSE listing (CSE: ACRG.U).
Acreage Holdings on its USD3.4 billion arrangement with Canopy Growth.
An Australian medicinal cannabis company in relation to its development and construction of a cannabis growing and processing facility.
A boutique retail chain on its own brand CBD cosmetic line and the legality of its products and their provenance across Italy, UK, Switzerland and France.
A syndicate of agents led by Canaccord Genuity in connection with:
Aurora Cannabis (TSX: ACB) USD230 million bought deal offering of convertible debentures.
CannaRoyalty s USD32.9 million offering of unsecured convertible debentures.
CannTrust Holdings (TSX: TRST) CAD100 million bought deal offering of units.
Golden Leaf Holdings CAD15 million bought deal private placement.
MedReleaf s CAD132.5 million bought deal offering of units.
Aurora Cannabis’ (TSX: ACB) USD230 million bought deal offering of convertible debentures.
CannaRoyalty’s USD32.9 million offering of unsecured convertible debentures.
CannTrust Holdings’ (TSX: TRST) CAD100 million bought deal offering of units.
Golden Leaf Holdings’ CAD15 million bought deal private placement.
MedReleaf’s CAD132.5 million bought deal offering of units.
Canaccord Genuity, in connection with Aurora Cannabis' (TSX: ACB) USD115 million special warrant offering.
A syndicate of underwriters, led by Canaccord Genuity, in connection with a USD40.3 million bought deal private placement of Supreme Pharmaceuticals Inc.'s (TSXV: FIRE) convertible debentures.
Charlotte's Web Holdings (CSE: CWEB) on its USD110 million IPO and CSE listing.
A developer of a medicinal cannabis delivery device in relation to the regulatory requirements of the Australian market, as well as in relation to corporate and tax issues.
Hanway Associates, the cannabis consultancy business, on the sale of HAPP Holdings Limited to NOBL Group, including the market-leading conference series Cannabis Europa.
HEXO Corp with its dual listing on the NYSE in addition to its TSX listing.
Materia Ventures on its expansion plans into Europe.
Newstrike Brands (TSX-V: HIP) in a share purchase agreement for interest in Neal Brothers Brands Inc. and joint venture agreement.
PharmaCielo Colombia Holdings on the legal structuring and implementation of its cannabis business in Colombia.
A producer of medicinal cannabis and cannabis oils on the Australian regulatory regime for cannabis and cannabis products, as part of an international project.
Trulieve Cannabis (CSE: TRUL) on its CAD65 million private placement of subscription receipts, reverse take-over of Schyan Exploration and CSE listing.
Defending a CBD company in a putative nationwide consumer class action filed in federal court alleging violations of state consumer protection laws based on the fact that all food, beverage, and nutritional supplements containing CBD are illegal, not proven to be safe, and a fraud and misrepresentation to the consuming public
Multiple CBD companies regarding interstate and cross-border shipment and exchange of CBD prototypes and samples, and use of CBD products in trade shows, including risk mitigation assessment
Supporting CBD companies seeking loans and financing as well as merchant payment support and tax filings in the context of the legal landscape and general education
Developing supply chain agreements, including manufacturing, co-manufacturing, distribution, retail, testing, and representations and warranties involving CBD products
Obtaining global patent protection for clients using CBD and cannabinoids for therapeutic treatments (eg, cancer)
Obtaining global patent protection for a client s new methods for extracting CBD from hemp
Attending hearings and committee meetings soliciting testimony and questions relating to current actions undertaken to permit the submission of hemp based CBD products for approval to FDA
Communication with USDA staffers regarding the Farm Bill, interpretation of Final Guidance as relating to key issues of testing, import, and certification as well as developing guidance
Defending a CBD company in a putative class action filed in federal court alleging violations of a state s consumer protection laws; it claims the company misstated the amount of THC in the CBD product (as zero THC), which allegedly resulted in the plaintiff failing a drug test and losing his job
Obtaining global patent protection for a client’s new methods for extracting CBD from hemp
Attending hearings and committee meetings soliciting testimony and questions relating to current actions undertaken to permit the submission of hemp based CBD products for approval to FDA
Communication with USDA staffers regarding the Farm Bill, interpretation of Final Guidance as relating to key issues of testing, import, and certification as well as developing guidance
Defending a CBD company in a putative class action filed in federal court alleging violations of a state’s consumer protection laws; it claims the company misstated the amount of THC in the CBD product (as zero THC), which allegedly resulted in the plaintiff failing a drug test and losing his job
Stefanie J. Fogel focuses her practice on multi-national food and consumer product regulation and compliance, food and consumer product recall response, corporate compliance, and commercial, class action and multi-plaintiff litigation.
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She works with large multinationals and start-ups in trending areas of the food and supplement space to include plant-based meat alternatives and hemp-based CBD products.
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Her clients include national and international manufacturers and retailers of foods, beverages, dietary supplements, cosmetics, and consumer goods, to include clothing, textiles and luxury products,
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She has extensive experience advising on FDA, USDA, TTB, and CPSC related regulations. She is also a seasoned trial lawyer, and has developed a global multidisciplinary crisis management team to address issues arising out of compliance issues, recalls, product contamination, and significant risks to Brand.
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Stefanie is the Vice Chair of AKD Partners's Markets and Sectors. She previously served as Co-Chair of the FDA Regulatory practice and as the Global Co-Chair of the Consumer Goods, Food & Retail Sector. Her leadership roles have also included serving on the firm's Policy Committee and the Hiring Committee.
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With our global team of insurance lawyers guiding you with pragmatic, strategic advice, you are primed for new opportunities, innovation, and responsible growth in the fast-moving insurance industry.
With a pragmatic approach and a steady hand, our global team executes the best dispute resolution strategies for your company. We are your partner in every sense of the word, fully invested in your success no matter where in the world you need us. \r\n
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With more than 25 years of experience as Senior Advisor in the Office of the Commissioner at the Food and Drug Administration (FDA), Sharon Mayl advises clients in the areas of food and ingredient safety, imports and exports, third-party audits, nutrition labeling, dietary supplements, infant formula, cosmetics, and cannabis products. She applies her insider experience to help clients navigate the black box of FDA, finding strategic and practical solutions to regulatory and compliance problems.
\n
Sharon provides strategic advice and regulatory counsel to clients in a variety of areas, including the FDA Food Safety Modernization Act (FSMA), Make America Health Again (MAHA) initiative, ingredient and product development, supplier verification, traceability, nutrition labelling and claims, infant formula, and dietary supplements. She also advises cosmetics clients on compliance with the Modernization of Cosmetics Regulation Act (MoCRA), labelling and safety issues. Sharon uses her decades of experience at the agency to assist clients with FDA interactions and meetings, including with respect to policy development and compliance actions such as warning letters and inspection reports.
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Sharon is a frequent conference speaker at industry conferences on a variety of topics including FSMA compliance, contaminants, MAHA and ultra-processed foods, dietary supplements, and navigating FDA's new Humans Foods Program. She also provides tailored training to clients and trade associations to facilitate regulatory compliance.
\n
During her time as Senior Advisor at FDA, Sharon counseled several deputy commissioners on a wide range of regulatory, legislative and policy issues. Sharon played a leading role in implementing FSMA and the Nutrition Labelling and Education Act, as well as developing FDA’s policies on imports and cannabis. Her role included significant rulemakings and she regularly represented the agency in meetings with senior administration officials, Congress, federal and state regulatory agencies, foreign governments, industry representatives and consumer and public health groups. Sharon established herself as a top government official in her space and forged close and cooperative relationships with a wide range of stakeholders to achieve solutions to novel, controversial and complex issues.
\n
Sharon has received numerous awards and distinctions for her public service, including the FDA Distinguished Career Service Award and the Commissioner's Award of Excellence for her outstanding contributions to the agency.
Stefanie J. Fogel focuses her practice on multi-national food and consumer product regulation and compliance, food and consumer product recall response, corporate compliance, and commercial, class action and multi-plaintiff litigation.
\n
She works with large multinationals and start-ups in trending areas of the food and supplement space to include plant-based meat alternatives and hemp-based CBD products.
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Her clients include national and international manufacturers and retailers of foods, beverages, dietary supplements, cosmetics, and consumer goods, to include clothing, textiles and luxury products,
\n
She has extensive experience advising on FDA, USDA, TTB, and CPSC related regulations. She is also a seasoned trial lawyer, and has developed a global multidisciplinary crisis management team to address issues arising out of compliance issues, recalls, product contamination, and significant risks to Brand.
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Stefanie is the Vice Chair of AKD Partners's Markets and Sectors. She previously served as Co-Chair of the FDA Regulatory practice and as the Global Co-Chair of the Consumer Goods, Food & Retail Sector. Her leadership roles have also included serving on the firm's Policy Committee and the Hiring Committee.
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With more than 25 years of experience as Senior Advisor in the Office of the Commissioner at the Food and Drug Administration (FDA), Sharon Mayl advises clients in the areas of food and ingredient safety, imports and exports, third-party audits, nutrition labeling, dietary supplements, infant formula, cosmetics, and cannabis products. She applies her insider experience to help clients navigate the black box of FDA, finding strategic and practical solutions to regulatory and compliance problems.
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Sharon provides strategic advice and regulatory counsel to clients in a variety of areas, including the FDA Food Safety Modernization Act (FSMA), Make America Health Again (MAHA) initiative, ingredient and product development, supplier verification, traceability, nutrition labelling and claims, infant formula, and dietary supplements. She also advises cosmetics clients on compliance with the Modernization of Cosmetics Regulation Act (MoCRA), labelling and safety issues. Sharon uses her decades of experience at the agency to assist clients with FDA interactions and meetings, including with respect to policy development and compliance actions such as warning letters and inspection reports.
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Sharon is a frequent conference speaker at industry conferences on a variety of topics including FSMA compliance, contaminants, MAHA and ultra-processed foods, dietary supplements, and navigating FDA's new Humans Foods Program. She also provides tailored training to clients and trade associations to facilitate regulatory compliance.
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During her time as Senior Advisor at FDA, Sharon counseled several deputy commissioners on a wide range of regulatory, legislative and policy issues. Sharon played a leading role in implementing FSMA and the Nutrition Labelling and Education Act, as well as developing FDA’s policies on imports and cannabis. Her role included significant rulemakings and she regularly represented the agency in meetings with senior administration officials, Congress, federal and state regulatory agencies, foreign governments, industry representatives and consumer and public health groups. Sharon established herself as a top government official in her space and forged close and cooperative relationships with a wide range of stakeholders to achieve solutions to novel, controversial and complex issues.
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Sharon has received numerous awards and distinctions for her public service, including the FDA Distinguished Career Service Award and the Commissioner's Award of Excellence for her outstanding contributions to the agency.
