FDA Regulations for Marketing Dietary Supplements in the U.S 2016

  • 27 Sep 2016
  • Webinar

Description

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

Past Events

Important

Please, check "FDA Regulations for Marketing Dietary Supplements in the U.S" official website for possible changes, before making any traveling arrangements

Event Categories

Government & Global Issues: Law & Regulations
Industry: Food & Beverages

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