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 » IRBs With Industry Studies May Need to Reregister
IRBs With Industry Studies May Need to Reregister
September 18, 2009
Institutional review boards (IRBs) that oversee FDA-regulated clinical trials and registered with the HHS Office for Human Research Protections (OHRP) before July 14 should check the OHRP database to see if their registration is correct.