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 » FDA Could Act Faster on AEs Under New Reporting System
FDA Could Act Faster on AEs Under New Reporting System
September 20, 2013
The FDA has chosen a long-awaited replacement for its outdated device adverse event reporting system — the Manufacturer and User Facility Device Experiences system, or MAUDE.