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.
In Collaboration with the
Our 2025 Conference Co-Chairs
Megan Olsen
Senior Vice President & General Counsel
Council for Responsible Nutrition
Taneesha Routier
Director of Regulatory Affairs
Xymogen
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.”
“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.”
“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.”
“Great content! It reinforced what I understood about the connection of regulations and litigation, while increasing my knowledge of quality and FDA audits.”
“Awesome opportunity to learn first-hand knowledge from those with expertise in the field of Dietary Supplements.”
“Comprehensive and in-depth review of leading regulatory issues for the dietary supplement industry.”
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]
