Consumer group criticizes FDA's medical device approval process

07/14/2010 | Hill, The

Researchers at consumer group Public Citizen have raised concerns about the FDA's process for approving medical devices, including regulators' interpretation of requirements for the 510(k) process and their concern that the new-device process is being bypassed. The authors urged a combination of legislation and regulatory changes.

View Full Article in:

Hill, The

Published in Brief:

SmartBrief Job Listings for Health Care

Job Title Company Location
Assistant General Counsel/Senior Corporate Counsel
Genentech
South San Francisco, CA
Senior Analyst Compliance
Edwards Lifesciences
Irvine, CA
Legal Counsel
Alcon
Fort Worth, TX
Director, Senior Legal Counsel
Alcon
Fort Worth, TX
Associate Director, Compliance Business Partner I
Boehringer Ingelheim
Ridgefield, CT