We use cookies to deliver our online services. Details of the cookies we use and instructions on how to disable them are set out in our Cookies Policy. By using this website you agree to our use of cookies. To close this message click close.

Postmarket Compliance: FDA is Connecting the Dots...Are You?

01 August 2006

Journal of Medical Device Regulation

Earlier this year, the U.S. Food and Drug Administration's (FDA's) Center for Devices and Radiological Health (CDRH) announced a new medical device postmarket safety programme intended to increase its ability to identify, analyse, and act on postmarket information. 


Loading data