Purchase any WEBINAR and get
10% Off
CODE: SAVE10
T&C applicable, please referFAQ
Validity : 15th Apr'24 to 25th Apr'24
FDA Regulation of Dietary Supplements in the U.S.A.
- FDA Regulations for marketing dietary supplements in the USA
- Dietary Supplement claims
- Marketing New Dietary Ingredients
- Dietary Supplement Labeling & Advertising rules
- Dietary Supplements GMPs
- FDA enforcement and Dietary Supplement Warning letters
Overview of the webinar
This presentation will provide an overview of FDA Dietary Supplement regulations with an emphasis on important regulatory requirements and dietary supplement claims and labeling. Dietary supplement controversies will also be covered.
Who should attend?
- Regulatory Affairs Managers and Associates
- Dietary Supplement Marketing Managers
- Nutritional Product Managers
- Anyone involved in marketing or labeling dietary supplement products in the USA
Why should you attend?
In order to market dietary supplements successfully in the USA and to avoid regulatory problems, it’s essential to understand US FDA dietary supplement regulations. This webinar will cover essential and significant 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 in 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.