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 ...
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 ...
The global Medical Device Contract Manufacturing market size was $73.61 billion in 2023 and is projected to reach $81.19 billion in 2024. This market is expected to grow significantly, reaching ...
Taiwan Semiconductor Manufacturing Company (TSMC) is planning a major move. The chipmaker is reportedly proposing a joint ...
A manufacturer produces a medical device for physicians to use to administer a particular type of treatment to their patients ...
The ubiquitous ESP32 microchip made by Chinese manufacturer Espressif and used by over 1 billion units as of 2023 contains ...
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 ...
Atlant 3D has raised $15 million as demand grows for its manufacturing system that builds materials and devices atom by atom.
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