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 » EU Device Directive Recast to Revise Notified Bodies Role
EU Device Directive Recast to Revise Notified Bodies Role
August 24, 2012
Revising the role and transparency of notified bodies in the EU’s medical device approval process could be the centerpiece of the European Commission’s recast of the medical device directives (MDD).