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How FDA & FTC Regulate Advertising & Promotion of OTC Drugs & Dietary Supplements
- How Dietary Supplement & OTC Advertising is regulated
- Dietary Supplement & OTC Drug Claims
- Dietary Supplement/OTC Drug Advertising Issues
- FTC substantiation standard
- FDA & FTC Warning Letters
- Targeted Enforcement Areas
Overview of the webinar
This webinar will help you understand the relationship between the FDA and the FTC and how they work together to review and regulate advertising and promotion of OTC drugs and dietary supplements. It will also convey an understanding of FTC’s substantiation standard and current enforcement actions against advertising and promotion that the FTC has targeted for violating regulations.
Who should attend?
- Director of Regulatory Affairs
- Regulatory Affairs Manager
- Regulatory Affairs Associate
- Marketing Manager
- Product Manager
Why should you attend?
In order to successfully market OTC Drugs and Dietary Supplements in the U.S. it is essential to understand how the FDA & the FTC regulate the advertising and promotion of these products. This webinar will provide an understanding of the compliance requirements of both agencies and how to successfully market one’s products while avoiding regulatory issues.
Faculty - Ms.Norma Skolnik
Norma Skolnik has over 35 years of regulatory experience working with the pharmaceutical and dietary supplement industries. She served as Director of Regulatory Affairs for the Americas for Cadbury Adams. Prior to that she was Director of Regulatory Affairs for the Adams Division of Pfizer and Associate Director Of Regulatory Affairs for the Warner-Lambert company. She also served as Director of Regulatory Affairs for Lederle Consumer Healthcare and as Associate Director of Marketed Product Support for Lederle Laboratories and Associate Director of Regulatory Affairs for Wyeth.