Center for Devices and Radiological Health, FDA
Dr. Minerva Hughes serves as the Regulatory Counsel for the Office of Clinical Evidence and Analysis in the Food and Drug Administration’s Center for Devices and Radiological Health, which provides policy and program oversight for clinical trials, biostatistics, real-world evidence, epidemiological analysis/safety surveillance, and FDA's Medical Product Safety Network. Dr. Hughes has over 15 years of experience in medical product development and FDA regulatory matters and has helped to advance several initiatives at the FDA to modernize the clinical research enterprise for more efficient product development. She received her doctorate degree from Johns Hopkins University and her law degree from the University of Maryland School of Law.
Wednesday, December 14, 2022
11:45 AM – 12:45 PM ET