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.
Hahn said the agency will distribute information to developers on approval pathways, such as Emergency Use Authorization, which allows the use of unapproved medical products in public health emergencies. Read More
NGS diagnostics can help patients and physicians put together a personalized cancer treatment plan because of the clinical information they provide. Read More
The FDA will hold a March 5 public workshop on evaluation practices for virtual and augmented reality in medicine at the agency’s White Oak Campus in Silver Spring, Maryland. Read More
Time is running out for devicemakers to meet the May 26 deadline to renew or extend their device certificates under the new EU Medical Devices Regulation, MedTech Europe stressed in its latest status report. Read More