IMDRF to issue updated medtech adverse events proposal soon

04/8/2014 | Clinica (subscription required)

The International Medical Device Regulators Forum has drafted a proposal to clarify and improve its program meant to allow regulators across the globe to share data on serious adverse events linked to medical devices. The proposal will be released for a 60-day comment period this month.

View Full Article in:

Clinica (subscription required)

Published in Briefs:

SmartBrief Job Listings for Health Care

Job Title Company Location
Director, Site Quality Management
Minneapolis, MN
In house Compliance Officer
Pompano Beach, FL
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