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Presentation

FDA CDRH Human Factors Regulatory Panel
DescriptionThis panel, featuring 3 FDA representatives, will discuss FDA regulatory issues, guidance, and best practices for the human factors of medical devices (CDRH).
Authors
Tania Reina
Assistant Director, Human Factors, Division of Drug Delivery and General Hospital Devices and Human Factors
U.S. Food and Drug Administration
Hannieybey D. Wiyor, Ph.D.
Human factors reviewer and consultant of regulated medical products
U.S. Food and Drug Administration
Michelle Shah
Biomedical Engineer
U.S. Food and Drug Administration
Event Type
Discussion Panel
TimeWednesday, March 2710:30am - 12:00pm CDT
LocationContinental Ballroom, Lobby Level
Tracks
Medical and Drug Delivery Devices