Federal Register Notice: CDRH will sponsor the 2016 Experiential Learning Program (ELP). The training component is intended to provide CDRH staff with an opportunity to understand the policies, laboratory practices, and challenges faced in broader disciplines that impact the device development life cycle. The Center is inviting medical device industry, academia, and health care facilities to request to participate in this formal training program for FDA’s medical device review staff, or to contact CDRH for more information on ELP. Requests should be submitted by 4/11. To view this notice, click here.