FDA to incorporate patient perspective into medtech reviews

07/31/2013 | MassDevice.com (Boston)

The FDA will conduct a public workshop on Sept. 18 and 19 to explore ways the agency's device center can incorporate patient preferences into evaluating the benefits and risks of medical devices. "Scientists, clinicians, device developers and regulators play critical roles in understanding the operation of medical devices and the associated benefits and risks. But only patients live with their medical conditions and need to make the choices required for their care," the agency said in a statement.

View Full Article in:

MassDevice.com (Boston)

Published in Brief:

SmartBrief Job Listings for Health Care

Job Title Company Location
Director, Site Quality Management
Minneapolis, MN
In house Compliance Officer
Pompano Beach, FL
Clinical Project Manager
Abiomed, Inc.
Danvers, MA
Sr. Manager, Regulatory Affairs - International
Integra LifeSciences
Plainsboro, NJ
Associate - Food and Drug
Keller and Heckman LLP
Washington, DC