Australia wants to conduct its own assessments of higher-risk devices

01/21/2013 | Clinica

Australia wants to add implantable devices and surgically invasive devices intended for long-term use to the list of products requiring a mandatory application audit by the country’s Therapeutic Goods Administration. The TGA also wants to allow Australian manufacturers of low-risk medical devices to use a European conformity assessment instead of requiring TGA scrutiny.

View Full Article in:

Clinica

Published in Brief:

SmartBrief Job Listings for Health Care

Job Title Company Location
Product Development Manager, Disposable Medical Products
ASAHI INTECC, Orange County CA R&D Center
Santa Ana, CA
Neurovascular Intervention Product Sales Rep, North East
ASAHI INTECC
Multiple Locations, SL_Multiple Locations
Vice President of Regulatory Affairs
Pentec Health
Boothwyn, PA
Sr Coordinator Clinical Research (US/TA/00/0073/SL) - 1400000AQX
Abbott
Santa Clara, CA
Senior Director, Biostatistics
Edwards Lifesciences
Irvine, CA