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Nearly a third of FDA medical device adverse event reports filed lateA new study found that 9.1% of medical device AEs were reported to the FDA 180 days later than required over a three-year ...
HealthDay News — Although most manufacturer reports of medical device adverse events are reported on time, a considerable proportion are submitted late, according to a study published online March 12 ...
AI-driven research is making titanium 3D-printing faster, stronger, and more efficient, transforming aerospace and defense ...
The National Association of Boards of Pharmacy (NABP) plays an important role in the state licensing of prescription medical device manufacturers ...
The Committee pointed out that several medical device manufacturers are hesitant to set up units in India due to the delaying ...
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 ...
Lithium-ion batteries are reaching a saturation point; so it's time for a new technology - Silicon carbon. Here's everything ...
Taiwan Semiconductor Manufacturing Company (TSMC) is planning a major move. The chipmaker is reportedly proposing a joint ...
Most medical devices in the United States come to market with limited clinical data, and device surveillance is viewed as a ...
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 ...
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