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 » Firms Should Track Unusual Sources of Device Complaints
Firms Should Track Unusual Sources of Device Complaints
August 24, 2007
The fastest way for medical device firms to get a warning letter is not to report adverse events to the FDA, according to Judith Andrews, director of quality and compliance services for Medical Device Consultants.