FDA aims to give reviewers an inside view of medtech development

04/4/2013 | MassDevice.com (Boston)

As part of its Experiential Learning Program, the FDA will send reviewers at the agency's device center to tour medtech facilities in an effort to help them better understand the device-development cycle and the hurdles faced by manufacturers from development to clinical testing. The agency is inviting medtech companies to register as hosts for the tours.

View Full Article in:

MassDevice.com (Boston)

Published in Briefs:

SmartBrief Job Listings for Health Care

Job Title Company Location
Vice-President of Technology and Regulatory Affairs
AdvaMed
Washington DC, DC
Sr Product Manager Global Marketing (US/DA/00/0085/SL) - 14000009V3
Abbott
Chicago, IL
Director of Medicare Products
Bluegrass Family Health
Lexington, KY
Director of Medicare Products
Bluegrass Family Health
Lexington, KY
Vice President, Information Technology
HealthPartners
MN