Senior Advisor for Patient Safety, Center for Devices and Radiological Health , FDA
Jay Crowley develops and implements new methods and techniques for identifying and resolving problems involving the use of medical devices. Mr. Crowley has held a variety of positions during his 20 years at the U.S. Food and Drug Administration (FDA). Currently, he has responsibility for implementing the Unique Device Identification requirements of the 2007 FDA Amendments Act. He holds a Master's degree in risk analysis and a Bachelor's degree in mechanical engineering.