Active surveillance using routine health data can improve patient safety The US Food and Drug Administration (FDA) requires manufacturers of medical devices, such as ventilators and defibrillators, to ...

Over 1.2 million medical device adverse event reports were not submitted to the US Food and Drug Administration (FDA) within the deadline set by federal regulations, finds an analysis of recent data ...

Jail video shows Sacramento County deputies and a nurse ignoring or mocking the clear medical problems of an inmate, who soon died of an overdose.

English AI model developed by KISTI to provide real-time infectious disease monitoring, bridging language gaps in public ...

Dwyane Wade, Kim Kardashian, Maria Menounos and Rick Springfield have touted full-body MRI scans. Should you get one?

Objective To describe the extent of late adverse event reporting by manufacturers to the US Food and Drug Administration’s (FDA) Manufacturer And User Facility Device Experience (MAUDE) database as ...