Minn. lawmakers air concerns over possible changes to 510(k) process

05/27/2010 | Pioneer Press (St. Paul, Minn.)

Sen. Amy Klobuchar, D-Minn., and Rep. Erik Paulsen, R-Minn., sent a letter to the FDA saying the proposed changes to the 510(k) process would stifle medical device innovation and result in unnecessary regulations for companies. Minnesota houses more than 400 medical-device firms that provide jobs for more than 50,000 people.

View Full Article in:

Pioneer Press (St. Paul, Minn.)

Published in Brief:

SmartBrief Job Listings for Health Care

Job Title Company Location
Chief Executive Officer
Center for Improving Value in Healthcare
Denver, CO
Quality Program Manager II, State Programs
Tufts Health Plan
Watertown, MA
Associate Director, Promotion Integrity
Bristol-Myers Squibb
Plainsboro, NJ
Vice President, Medicare Advantage
BCBS-Louisiana
Baton Rouge, LA
Director, Global Integrity and Compliance, Pharmaceuticals
Alcon
Fort Worth, TX