Special emergency treatment units have been set up in primary health centres and hospitals across the state to manage cases ...

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 ...

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

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

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 ...

Debates over tuberculosis reporting began in the late 19th century, when the bacterial infection was reframed not as a disease of the elite but of the urban poor. New York City was the first in the ...

According to Dr Bahizi, the initial four suspected cases originated from Ntoroko District, while the two new cases involve ...