FDA-Health Professional Activities
Learn about current FDA programs that involve health professionals.
Health professionals, consumers and patients can voluntarily report observed or suspected adverse events for human medical products to FDA. Voluntary reporting can help FDA identify unknown risk for approved medical products.
Learn MoreFDA Updates Regulations on Mammography - June 2019
Learn MoreMar 25
Medical Devices, Radiation-Emitting Products
Mar 25
Medical Devices
Mar 19
Medical Devices