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.
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.
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.
Areas Covered in the Webinar:
- Dietary Supplement labeling.
- FDA requirements for Principal Display Panel.
- FDA requirements for Supplement Facts box.
- Other statutory and regulatory labeling requirements.
- Types of dietary supplement claims.
- Unqualified health claims.
- Qualified health claims.
- Structure-Function claims.
- Nutritive value claims.
- Claim substantiation.
- Clinical and nonclinical studies.
- Truthful and non-misleading advertising.
- FDA and FTC standards.
- Ingredient Review
- What is GRAS?
- When is Pre-market approval required?
- Factors to distinguish conventional foods, like sodas, from liquid dietary supplements, like energy or melatonin drinks.
Who Will Benefit:
- Food & beverage industry executives
- Dietary Supplement manufacturers/distributors
- Medical Device manufacturers/distributors
- In-House Legal Counsel
- Regulatory Affairs
- Government Affairs
- Distributors and manufacturers
- Customs brokers
- FDA/Food & Drug Attorneys
Course Provider
Marc Sanchez,
