FDA outlines key medical device projects for 2013

05/5/2013 | Clinica

In an effort to bolster its post-market surveillance of medical devices, the FDA will focus on five projects that include creating a planning board for the post-market surveillance system and finalizing rules for a unique device identification system. In addition, the FDA will encourage the creation of national and international registries for certain products, modernize the reporting and analysis of adverse events and develop and implement new methods.

View Full Article in:


Published in Briefs:

SmartBrief Job Listings for Health Care

Job Title Company Location
Santa Ana, CA
Regulatory Analyst
Delta Dental
Alpharetta, GA
Eastern Zone Sales Director
Regenesis Biomedical
White Plains, NY
Senior Financial Analyst - Growing Manager Care Health Org
Fallon Community Health Plan
Worcester, MA
Associate Director, Regulatory Affairs - Promotional Review
Novo Nordisk
Princeton, NJ