The FDA has launched a new web page that will keep the public informed about the status of post-approval patient studies for certain recently approved medical devices. “FDA is committed to improving its medical device safety program and ensuring that medical devices remain safe and effective once they are in the hands of health professionals and the public,” said Daniel Schultz, M.D., director of FDA’s Center for Devices and Radiological Health. “Electronic access will give the public an opportunity to see progress being made on a company’s post-market commitments.” Information: www.accessdata.fda.gov.
Post-Approval Patient Studies Site
Mon, 05/14/2007 - 7:06am