FDA CDRH Experiential Learning Program is open for comments

April 3, 2017

The Food and Drug Administration’s (FDA) Center for Devices and Radiological Health (CDRH) announced on March 23, 2017 that the submission period for Experiential Learning Program (ELP) in open.

ELP is a training component intended to provide CDRH staff with an opportunity to understand the policies, laboratory practices, patient perspective/input, quality system management, and other challenges that impact the device development life cycle.

CDRH ELP – 2017 Federal Register Notice is intended to invite medical device industry, academia, and health care facilities, and others to participate in this formal training program for CDRH’s employees, or to contact CDRH for more information regarding the ELP (see link below for more detail).

Submit either electronic or written requests for participation in the ELP by dates specified in the ELP Web site at: http://www.fda.gov/scienceresearch/sciencecareeropportunities/ucm380676.htm.

 Current Submission Period Status: OPEN
Submission Period: March 23, 2017- April 30, 2017
Proposal Submission Location Link:
ELP – 2017 Federal Register Notice