Medical Device Network on MSN21h
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 ...
The National Association of Boards of Pharmacy (NABP) plays an important role in the state licensing of prescription medical device manufacturers ...
StockStory.org on MSN1d
Q4 Earnings Roundup: CooperCompanies (NASDAQ:COO) And The Rest Of The Medical Devices & Supplies - Diversified SegmentWrapping up Q4 earnings, we look at the numbers and key takeaways for the medical devices & supplies - diversified stocks, ...
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 ...
It was imperative for a large European CMO that produces multiple biologic drugs to select the right product quality and ...
The Federal Trade Commission has filed a lawsuit to block private equity firm GTCR BC Holdings from acquiring Surmodics, a medical technology company, arguing the deal would reduce competition for ...
Medical Device Network on MSN7d
Cerus secures CE mark approval for LED-based illumination deviceCerus Corporation has secured CE mark approval for its INT200, a LED-based illumination device, for the Intercept Blood ...
The UK Government has accepted most of the recommendations of the Regulatory Horizons Council (RHC) on the regulation of AI in medical devices.
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