Report outlines proposed changes to EU medtech regulation

04/17/2013 | Clinica (subscription required)

A draft report released Monday by the European Parliament details proposed changes to the medical device regulation in Europe, including creating both centralized and decentralized premarket approval processes for medical devices and making it difficult for device makers to classify their products as single use. The proposals are expected to draw opposition from the industry, according to this article.

View Full Article in:

Clinica (subscription required)

Published in Briefs:

SmartBrief Job Listings for Health Care

Job Title Company Location
Senior Director, Research
America's Health Insurance Plans (AHIP)
Washington, DC
Sr. Principal OptoMechanical Engineer - 14000008M2
Abbott
San Jose, CA
Pharmacy Care Manager
National Association of Chain Drug Stores
Arlington, VA
Regional Director, Southeastern Region - State Affairs
America's Health Insurance Plans (AHIP)
Washington, DC
Sr. Principal Electrical Engineer - 14000008LR
Abbott
San Jose, CA