FDA makes alarm fatigue an issue in new device approval process

03/27/2012 | Boston Globe (tiered subscription model), The

The FDA said it will provide more training on the safety issues of alarm fatigue to staff who evaluate approval applications for medical devices in hospitals. The FDA will also consider whether alarms on new devices actually provide information important to patient care.

View Full Article in:

Boston Globe (tiered subscription model), The

Published in Briefs:

SmartBrief Job Listings for Health Care

Job Title Company Location
Director of Clinical Operations
Meridian Health Plan
Detroit, MI
Sr. Director, Regulatory Compliance Intelligence and Outreach
Johnson & Johnson
New Brunswick, NJ
RN Care Manager
MJHS
Brooklyn, NY
Director of Utilization Management
Meridian Health Plan
Chicago, IL
Senior Manager, Healthcare Reform
Avalere Health
Washington, DC