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  • Dietary Supplements Ingredient and Labeling Compliance

  • Hosted By:
  • ComplianceOnline
  • Start:
  • Tuesday - Jul 09, 2013 10:00 AM
  • End Time:
  • Tuesday - Jul 09, 2013 11:00 AM
  • Location:
  • Online
  • This webinar on dietary supplements will cover product ingredient reviews and FDA requirements for labeling your products in the US. You will learn how to avoid claims, what claims are permissible and how to remedy challenged claims.

    Why Should You Attend:

    - What is the risk exposure from product ingredients?
    - What risks typically stem from labeling and marketing dietary supplements?
    - How to distinguish conventional foods from liquid dietary supplements?
    - What is the boundary between the FDA and the FTC?

    The expansion of product offerings in the Dietary Supplements category has been met by an increase in FDA monitoring and enforcement. It is therefore important for dietary supplement companies to ensure their product labels and accompanying claims are fully compliant with applicable statutes and regulations.

    This webinar will cover how dietary supplement companies should label their products for the US market per FDA requirements, considerations to avoid claims, building regulatory compliance into company programs for development and launch of properly labeled dietary supplements. You will learn what claims are permissible, what constitutes a disease or drug claim, the implications of making impermissible claims and how to remedy challenged claims. We will also look at ingredient reviews and factors to distinguish conventional foods and liquid dietary supplements, like energy drinks.
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