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 » Input Sought on U.S. FDA Device Audit Plan, Assessment Slated for Summer
Input Sought on U.S. FDA Device Audit Plan, Assessment Slated for Summer
January 9, 2013
The U.S. Food and Drug Administration (FDA) is seeking industry comment in advance of an independent audit of the Center for Devices and Radiological Health’s premarket review processes — one of the agency’s Medical Device User Fee Act (MDUFA) III commitments.
To View This Article:
Login
Subscribe To International Medical Device Regulatory Monitor