Speaker - Steven Gutman

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Steven I. Gutman is Director of the Office of In Vitro Diagnostic Device Evaluation and Safety at the Food and Drug Administration (FDA). A board certified pathologist, Dr. Gutman has served as an FDA regulator for the past 15 years in the area of laboratory tests, referred to by the FDA as in vitro diagnostic devices. He was appointed Director of the office he now oversees in 1993, the year the office was created. Before that Dr. Gutman was Director of the FDA's Division of Clinical Laboratory Devices, where he had previously served as a medical officer.

1 Program

Tailor-Made Medicine

10.06.07 | 01:20:59 min | 0 comments