Australia creates database on adverse events tied to medtech

06/23/2013 | Clinica

The Therapeutic Goods Administration in Australia has introduced the Database of Adverse Event Notifications for medical devices, which includes data on adverse events reported to the TGA since July of last year. The database is part of an effort to form the Australia New Zealand Therapeutic Products Agency, a regulatory body that would link the TGA with its New Zealand counterpart.

View Full Article in:

Clinica

Published in Briefs:

SmartBrief Job Listings for Health Care

Job Title Company Location
Director, Senior Legal Counsel
Alcon
Fort Worth, TX
Associate Director, Compliance Business Partner I
Boehringer Ingelheim
Ridgefield, CT
Attorney
U.S. DEPARTMENT OF HEALTH & HUMAN SERVICES Food and Drug Administration Office of the Chief Counsel
Silver Spring, MD, MD
Counsel – Regulatory Affairs
RAI Services Company
Winston Salem, NC
Senior Manager, Clinical Affairs - Advanced Technology
Edwards Lifesciences
Irvine, CA