FDA pushes for electronic reporting of adverse events

08/20/2009 | Modern Healthcare (free registration)

The FDA proposed regulations that would mandate companies to electronically file reports of adverse events linked to approved medical devices, drugs and biotech items. The agency hopes the rules will reduce industry costs and streamline communication between the FDA and other federal agencies.

View Full Article in:

Modern Healthcare (free registration)

Published in Brief:

SmartBrief Job Listings for Health Care

Job Title Company Location
Clinical Project Manager
Abiomed, Inc.
Danvers, MA
Sr. Manager, Regulatory Affairs - International
Integra LifeSciences
Plainsboro, NJ
Associate - Food and Drug
Keller and Heckman LLP
Washington, DC
Market Access Manager Electrophysiology HEOR (AEP) - 15000003NZ
Abbott
Menlo Park, CA
Sales Manager, Employer Programs
PartnerRe Health