Manufacturing engineers are the background force behind successful medical device coatings, ensuring precision, consistency, ...
XBeta founder Frederick Kruger offers advice for medical device startups based on his firm's development of the Spiro Wave ...
Manufacturers urge the govt to review medical device tariffs as the Centre considers cutting import duties on them in India.
The National Association of Boards of Pharmacy (NABP) plays an important role in the state licensing of prescription medical device manufacturers ...
BD, Medtronic and Abbott were among the top 10 device companies with the highest number of late reports to the FDA, the study ...
Creative Foam makes custom-engineered die-cut, formed foam, nonwoven and multi-material component solutions to medtech ...
Most medical devices in the United States come to market with limited clinical data, and device surveillance is viewed as a ...
Under federal law, device makers must submit adverse event reports they receive from patients to the FDA’s Manufacturer And User Facility Device Experience (MAUDE) database within 30 days, researchers ...
The regulatory environment for prescription medical device manufacturers and distributors has become increasingly stringent as state-based ...
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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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 ...
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