A final rule issued by the U.S. Food and Drug Administration will require reports on medical device adverse events to be submitted electronically, beginning Aug. 14, 2015.
Read the full story on Becker's Hospital Review.
University of Michigan Health Startup Receives FDA Clearance for Patient Monitoring Software
Polymicro Technologies Achieves FDA Quality System Regulation Registration, Compliance
Ziehm Imaging Announces FDA Clearance for C-Arm Imaging Solution
Read the full story on Becker's Hospital Review.
More Articles on the FDA:
University of Michigan Health Startup Receives FDA Clearance for Patient Monitoring Software
Polymicro Technologies Achieves FDA Quality System Regulation Registration, Compliance
Ziehm Imaging Announces FDA Clearance for C-Arm Imaging Solution