Simplifying Global Compliance
FDA Asks TV Mesh Manufacturers to Conduct Postmarket Studies
Devices & Diagnostics Letter
Surgical mesh manufacturers have until Feb. 3 to submit their plans to the FDA for conducting postmarket studies under Section 522 of the 1938 FD&C Act.
To View This Article:
Buy This Article Now
Copyright ©2016. All Rights Reserved.
Design, CMS, Hosting & Web Development :: ePublishing