Dr. Susan Alpert, PhD, MD
Susan Alpert, Ph.D., M.D.is specializes on the strategies needed to place medical devices and other medical products into the global market.
She was a Corporate Senior Vice President for Global Regulatory at Medtronic, Inc. and prior to that VP Regulatory Science at C.R. Bard, Inc. She worked at the US FDA from 1987-2000 where she held a variety of management positions in the Centers for drugs, devices and radiological health, and foods.
She was Director of the Office of Device Evaluation from 1993-1999. Susan chaired the RAPS board was on the boards of FDLI, WBL and SWHR.