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.
A new report from the Duke-Margolis Center for Health Policy is offering an initial peek into a planned coordinating center intended to guide the development and implementation of a postmarket device evaluation system. Read More
With an eye toward making the conduct of clinical studies more efficient, the FDA and NIH have unveiled a template intended for investigators writing Phase 2 or 3 trial protocols that require IDE applications. Read More
Two House members are calling on HHS Secretary Sylvia Burwell to provide more details of how the department is responding to the Zika outbreak, saying the current status of diagnostic testing for the virus is alarming. Read More
European officials are roughly 90 percent of the way toward reaching an agreement on new regulations for medical devices and in vitro diagnostics, but there are still points of contention, according to one expert. Read More