Seeking Proposals for Site Visits for CDRH Regulatory Staff Training

The U.S. Food and Drug Administration (FDA) invites medical device companies, health care facilities, and academia to submit proposals as part of the CDRH Experiential Learning Program (ELP) for regulatory review staff.  ELP is a formal training mechanism for CDRH regulatory review staff to visit research, clinical, manufacturing, and health care facilities to observe how medical devices are designed, developed, and used.    The submission period for proposals is: Start date: Friday, January 24, 2020 End date: Monday, February 24, 2020 at 12:00 p.m. EST

Learn about training needs and the submission process Questions? For questions about the Experiential Learning Program, including information about submitting proposals, email the ELP Program Manager at elp@fda.hhs.gov or phone 240-402-2246.