Ms. Norma Skolnik

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Profile

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.

3 results Found
Recorded Webinar

OTC Drug Safety, Innovation and Reform Act

The OTC Reform Act will have a huge impact on all companies in the OTC drug industry and companies need to learn about this Act. This Act will bring many changes to the OTC Monograph system and it’s essential that companies understand these ...

  • 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 subs ...

  • Basic & Intermediate
  • 60 Mins