Gail Pilgrim claims the longest tenure in Temple’s QA/RA program, creating the Food and Drug Law I course in 1984. As a consultant, she specializes in the regulation of research, development and marketing of pharmaceuticals. Previously she practiced FDA regulatory law for Rorer Group, Inc., and Burroughs Wellcome Co. She holds an AB, summa cum laude, and an MA from Bryn Mawr, a JD from the University of Pennsylvania, and a post-graduate LLM in Food and Drug Regulation from New York University. There she conducted research in patient labeling and pharmaceutical industry innovation and competition. She was a contributing author to SCRIP Reports: The Guide to GCP in the USA, and has spoken for FDLI and the PhRMA Education and Research Institute. She participates in on-site training about clinical contracting and product promotion to top pharmaceutical firms.

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