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 » Innovation, Faster Reviews Top U.S. FDA Device Goals in 2012
Innovation, Faster Reviews Top U.S. FDA Device Goals in 2012
March 1, 2012
The U.S. Food and Drug Administration plans to begin triaging premarket submissions April 1, in an effort to improve efficiency and strengthen premarket reviews.
To View This Article:
Login
Subscribe To International Medical Device Regulatory Monitor