ACI and CRN are excited to welcome you back to New York City this Spring for our 13th Legal, Regulatory & Compliance Forum on Dietary Supplements.

Join us at this year’s conference to better understand how the new Administration will impact your business operations, and to obtain critical updates on the latest legal, regulatory, and policy developments that will impact industry practices for the remainder of 2025 and beyond.

American Conference Institute

In Collaboration with the

Council for Responsible Nutrition | The Science Behind the Supplements

2025 Agenda Highlights

Impacts of the Current Administration on the Dietary Supplements Industry: Adapting Your Business to New Challenges and Opportunities

Navigating the Implications of New Trump Tariffs on Global Ingredient Sourcing and Supply Chain Operations

Meeting Dietary Supplement Company Obligations Under New Extended Producer Responsibility Laws

Adhering to Ramped-Up State Legislation Including New Age Restriction Laws, Ingredient Bans and Health Privacy Laws

Dietary Supplement Advertising Essentials: The Latest in Green Claims, Health Claims, and Navigating the FTC’s Final Rule on Endorsements, Testimonials and Consumer Reviews

Maintaining Compliance in the Online Marketplace: Navigating Requirements of Supplement Retailers and Combatting Counterfeits and Other Threats

Keeping Up with Emerging Class Action Activity and Trends Posing Threats to the Dietary Supplements Industry

Leveraging AI in Dietary Supplement R&D: Harnessing Innovation While Navigating Key Regulatory and IP Risks

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 More
“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
“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
“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
“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

Questions?

Email us at [email protected]

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