Most Americans are unaware of the complex process behind drug approval. Dr. Gordin’s presentation traces a medication’s journey from discovery and testing through FDA review, highlighting key historical events that shaped modern drug safety regulations.

About the speaker: M. Daniel Gordin, Ph.D. is a retired regulatory affairs executive with 40+ years in pharmaceutical development, including FDA service, and now advises biotechnology startups through SCBio.

FREE for JCC Member; $15 Nonmember