We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
Accept
Home » CDRH Working on MDR Protocol in Response to OIG Evaluation
CDRH Working on MDR Protocol in Response to OIG Evaluation
November 5, 2009
Devicemakers may see more action taken on late and incomplete medical device reports (MDRs) as CDRH develops a protocol addressing concerns raised in a
new report by the HHS Office of Inspector General (OIG).