In order to successfully market dietary supplements in the U.S. it’s essential to understand FDA regulations and trends in FDA regulation and enforcement of supplements through FDA dietary supplements training.
Why Should You Attend:
This webinar will help participants understand dietary supplement health and education act, FDA regulations for dietary supplements and how to avoid regulatory problems.
Areas Covered in this Webinar:
Background and History of the Dietary Supplement Health and Education Act
How Dietary Supplements can be Marketed in the U.S. in Compliance with FDA Regulations
Overview of Structure/Function Claim Regulations
Dietary Supplement Labeling Requirements
Summary of Dietary Supplement GMP Regulations
FDA Rules for Adverse Event Reporting of Dietary Supplements
Why Dietary Supplement Firms get FDA updates and Warning Letters and How to Avoid Them
Who Will Benefit:
Regulatory Affairs Managers
Directors and Associates
Anyone planning to market or import dietary supplements into the U.S.
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.
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