Biography:

Norma Skolnik is a regulatory consultant to FDA-regulated companies and firms wishing to launch products in the U.S.A. Norma has over 35 years of U.S. regulatory experience, starting in the pharmaceutical industry. She was the Associate Director of Regulatory Affairs at Lederle Laboratories in Pearl River, N.Y. Then she became Associate Director of Regulatory Affairs at Lederle Consumer Health, where she helped launch Centrum and Caltrate dietary supplements. When Wyeth acquired Lederle, she became Associate Director of Regulatory Affairs there, acquiring more experience in the Dietary Supplement and OTC drug fields. She joined Warner-Lambert Consumer Health division in 1998 and became Assistant Director of Adams Regulatory Affairs. In 2002, when Pfizer acquired Warner-Lambert, she was promoted to Director of Regulatory Affairs for the Adams division. Cadbury-Schweppes acquired Adams in 2003, and she served as Cadbury Adams' Director of Regulatory Affairs for the Americas from 2003 until her retirement in 2008.

Norma earned a Bachelor's in Biology from the University of Cincinnati and a Master's from Pratt Institute in Brooklyn, New York. She's also done graduate work at Columbia University and Montclair State University.