Industry Input On Device Trial Database To Be Sought By CDRH In June
This article was originally published in The Gray Sheet
Executive Summary
FDA plans to solicit the viewpoints of device manufacturers within the next two weeks on the feasibility of including information on device clinical trials in a public database coordinated by the National Institutes of Health, FDA staffers report. The agency also plans to discuss the issue at a July 8 public forum, which will formally be announced in the near future.