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 » Increased Global Focus in U.S. FDA Device Compliance Office Restructure
Increased Global Focus in U.S. FDA Device Compliance Office Restructure
The U.S. Food and Drug Administration has created a new Division of International Compliance Operations to oversee inspections of foreign devicemakers and the international audit program.
To View This Article:
Login
Subscribe To International Medical Device Regulatory Monitor