ACI and CRN are excited to welcome you back to New York City this Summer for our 15th Legal, Regulatory & Compliance Forum on Dietary Supplements
As 2026 continues to unfold and we prepare for 2027, dietary supplement companies are no longer preparing for change — they are operating in a constant state of regulatory, enforcement, and policy evolution. This forum is designed for the industry’s top legal, regulatory, and business professionals to provide clarity, strategy, and practical solutions in the face of ongoing disruption and uncertainty. Previous discussion topics included the proposed overhaul of GRAS determinations, drug preclusion, NDIN guidance, supplement oversight modernization, tariff turbulence, EPR requirements, ingredient bans, using AI in compliance operations, claim substantiation, and more.
The 2027 is currently under development – Be first to hear about program and event updates and upcoming promotions by joining our mailing list.
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In Collaboration with the
Advisory Board
Meet the distinguished Advisory Board behind our industry leading Legal, Regulatory, and Compliance Forum on Dietary Supplements. Comprising of leading legal and industry professionals, they bring unique insights to crafting an agenda focused on innovation, impact, and meaningful discussions centered on the industry’s business operations and best practices.
View Advisory Board
A Must-Attend Event For
Dietary Supplement Industry Representatives:
- In-House Counsel, including generalists and those having responsibility for FDA and FTC compliance and regulatory affairs as well as:
- Advertising and Promotion
- IP, Patents and Trademarks
- Licensing and Business Development
- Officers, Directors and Executives for Regulatory Affairs and Business Development
Law Firm Attorneys for the Dietary Supplement Industry whose practices focus on:
- FDA and FTC law
- Advertising and Promotion
- Trademarks, Patents and IP
CLE Accreditation
Accreditation will be sought in those jurisdictions requested by the registrants which have continuing education requirements. This course is identified as non-transitional for the purposes of CLE accreditation.
Learn MoreTestimonials
“Great content! It reinforced what I understood about the connection of regulations and litigation, while increasing my knowledge of quality and FDA audits.”—Senior Global Regulatory Affairs Manager, Unilever
“As a member of a dietary supplement regulatory affairs department reviewing product content daily for FTC / FDA compliance, it was a valuable experience to be in a room with top minds from around the country who could answer my questions.”—Regulatory Associate, FoodState
“I appreciated the attention to urgent regulatory concerns, the application to personalized nutrition, and specifically – how each presenter tied it back to what companies can do to protect themselves and the industry.”—Medical Operations Manager, Fullscript
“I really enjoyed the ability to interact, converse and network with the speakers as well as the other attendees to discuss their experiences and knowledge in these areas of the Supplements industry. The wide range of topics and knowledge was impressive.”—Paralegal, Vitaquest
“Awesome opportunity to learn first-hand knowledge from those with expertise in the field of Dietary Supplements.”—Director of R&D/Quality, NutraBlend Foods
“Comprehensive and in-depth review of leading regulatory issues for the dietary supplement industry.”—Chief Operating Officer, Universal Nutrition
Sponsors & Partners
Sponsor Opportunities
With conferences in the United States, Europe, Asia Pacific, and Latin America, the C5 Group of Companies: American Conference Institute, the Canadian Institute, and C5 Group, provides a diverse portfolio of conferences, events and roundtables devoted to providing business intelligence to senior decision makers responding to challenges around the world.
For more information please contact:
Jason Kanagalingam
Business Development Manager
Phone: 647-649-2438
Email: [email protected]
