International Medical Device Regulatory Monitor

May 2012 | Vol. 20 No. 5

Developed, Developing Nations Should Work in Tandem to Ensure Safe Imports

The U.S. Food and Drug Administration (FDA) and other agencies must provide expertise, training and tools to developing nations to improve their device and drug monitoring practices and prevent dangerous healthcare products from entering the U.S., according to an April 4 Institute of Medicine (IOM) report.

This article is viewable by subscribers only. To view this article, please select an option below.

Subscribe
Print This Page
RSS
Free Trial
Archives
Sample PDF

Briefs Efforts to Map Global UDI System Benefit From FDA First Steps Restructuring of U.S. FDA Device Office Aimed at Furthering Foreign Focus FDA, Health Canada Say Robust Recall Plans Needed

Home
Advertising/Sponsorships
About Us
Contact Us
Site Map
Privacy Policy

300 N. Washington St., Suite 200, Falls Church, VA 22046, USA.
Phone (703) 538-7600 - Fax (703) 538-7676 - Toll free (888) 838-5578.