Assistant Director, Establishment Assessment Team 1, Office of Regulatory Programs, Office of Product Evaluation and Quality (OPEQ), Center for Devices and Radiological Health (CDRH) FDA (Invited)
Hear about CDRH’s strategic priorities, new initiatives, and ongoing work. Dr. Michelle Tarver, Center Director, will provide her insight on several activities underway at CDRH, including the Home as a Health Care Hub, the Communications Pilot to Enhance the Medical Device Recall Program, Medical Device User Fee Amendments (MDUFA) update, the Total Product Life Cycle Advisory Program (TAP) pilot, medical device cybersecurity, the Digital Health landscape, and more. You won’t want to miss it!
