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 Guideline Tackles IVD Borderline, Classification Issues
EU Guideline Tackles IVD Borderline, Classification Issues
March 1, 2012
The European Commission has published a final guideline aimed at clarifying borderline and classification issues related to in vitro diagnostic (IVD) devices.
To View This Article:
Login
Subscribe To International Medical Device Regulatory Monitor