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Ms.Norma Skolnik
Area Of Expertise : FDA
30 Years Of Experience
Training Industry : Life Sciences
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.
2 results Found
On-Demand Webinar
Gmo Food Labeling In The U.S.A. What To Expect From The Final Rule
The USDA recently unveiled its long-awaited proposed GMO Labeling Disclosure regulation, the National Bioengineered Food Disclosure Standard, which provides food companies with guidance about how to label products made with genetically modified ingredients. Th ...
- Basic & Intermediate
- 60 Mins
On-Demand Webinar
How FDA & FTC Regulate Advertising & Promotion of OTC Drugs & Dietary Supplements
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 ...
- Basic & Intermediate
- 60 Mins