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 » Guidance Clarifies Common Concerns in IVD Device Studies
Guidance Clarifies Common Concerns in IVD Device Studies
December 12, 2007
The U.S. Food and Drug Administration (FDA) has released a new draft guidance to help device manufacturers and clinical trial personnel develop in vitro diagnostic (IVD) studies.
To View This Article:
Login
Subscribe To International Medical Device Regulatory Monitor