FDA Regulations for Marketing Dietary Supplements in the U.S 2016 is a webinar that covers topics such as:
- DSHEA: How it changed FDA`s role in supplement claims & labeling
- Dietary Supplement Health & Education Act (DSHEA)
- Dietary supplement controversies
- U.S. Dietary Supplements
- Food Safety & Modernization Act/ Dietary supplement registration requirements
- FDA dietary supplement regulatory enforcement priorities
- Dietary Supplement claims / health claims
- Bioterrorism Act requirements
- Dietary supplement labeling
- FDA disclaimer required for structure/function claims
- Conventional Food vs. Dietary Supplement
- Why so much controversy?
- Requirements for Dietary Supplements vs. Foods
- 2014 Final guidance documents on beverages and dietary supplements
- Dietary supplement Good Manufacturing Practices (GMPs)
- Points to consider if marketing a dietary supplement in the USA
- What to expect in the near future
- Is it a dietary supplement? What`s your opinion?
FDA Regulations for Marketing Dietary Supplements in the U.S 2016 is intended for:
- Directors & associates
- Regulatory affairs managers
- Marketing managers and anyone planning to market, label or promote dietary supplements in the U.S
- Compliance specialists