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Marketing Dietary Supplements in Compliance with FDA Regulations
- FDA Regulations for Marketing Dietary Supplements in the US
- New Dietary Ingredients
- Dietary Supplement Labeling & Advertising Regulations
- Dietary Supplement GMP Regulations
- FDA Enforcement & Warning Letters
Overview of the webinar
This webinar will cover essential and significant FDA regulatory requirements for the marketing and labeling of U.S. dietary supplements. It will also cover how to market a product with a new dietary ingredient, permissible dietary supplement claims and their requirements, FDA registration requirements, dietary supplement promotional claims and ways to avoid regulatory challenges that could result in a company receiving an FDA Warning Letter.
Who should attend?
- Regulatory Affairs Managers & Associates
- Labeling Managers
- QA Managers
- Marketing Managers
Why should you attend?
In order to market Dietary Supplements successfully in the USA and to avoid regulatory problems, it is essential to understand US FDA Dietary Supplement regulations. This webinar will cover essential and significant FDA regulations for the marketing and labeling of US dietary supplements. It will also cover permissible dietary supplement claims and ways to avoid regulatory challenges that could get a company into trouble.
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.