How the FDA & FTC Regulate Advertising & Promotion of Drugs & Dietary Supplements
This webinar will cover FDA regulatory compliance training requirements for all manufacturers and distributors who want to advertise and/or promote OTC drugs list and dietary supplements in the U.S. The relationship between FDA and the FTC will be covered.
Why Should You Attend
In order to market dietary supplements and OTC drugs in the U.S.A., it’s essential to understand FDA guidelines and FTC rules and regulations and guidelines for advertising and promotion and to comply so as to avoid any regulatory problems.
Areas Covered in this Webinar
Learn about the role of the National Advertising Division (NAD)
Review the types of regulated advertising and promotion (TV, radio, internet ads, print ads, etc.) and regulatory requirements
Learn how to avoid getting FDA and FTC Warning Letters
Learn about competitive challenges
Understand the relationship of FDA and FTC in regulating consumer advertising
Understand what product claims are acceptable for advertising and promotion of dietary supplements and OTC drugs
Who Will Benefit
Regulatory Affairs Managers
Directors and Associates
Advertising Agency Representatives
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.