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Nathan Reeves on Food and Drug Administration (FDA) | JD Supra
JD Supra· 14 hours agoJD Supra is a legal publishing service that connects experts and their content with broader audiences of professionals, journalists and associations. This ...
San Diego's Cue Health had the first FDA-approved home COVID-19 test. Now the agency says to throw...
U-T San Diego· 1 day agoThe U.S. Food and Drug Administration told consumers Monday to throw out any at-home COVID-19 tests...
FDA recalls Abbott’s HeartMate 3 ventricular assist device after 2 deaths
Medical Device Network via Yahoo Finance· 4 hours agoThe US Food and Drug Administration (FDA) has tagged a recall of Abbott’s HeartMate 3 left...
Throw out COVID-19 tests made by Cue Health, FDA warns
WPIX New York City, NY via Yahoo News· 7 hours agoSAN DIEGO (KSWB/KUSI) — The U.S. Food and Drug Administration is warning people not to use COVID-19...
FDA report highlights need to improve diversity in clinical trials
Clinical Trials Arena via Yahoo Finance· 7 hours agoThe US Food and Drug Administration’s (FDA) Center for Drug Evaluation
Axogen begins FDA submission for nerve graft product By Investing.com
Investing.com· 6 hours agoAxogen, Inc. (NASDAQ: AXGN), a company specializing in surgical solutions for peripheral nerve...
Ventilator recall issued with warning of "serious injuries or death"
Newsweek· 1 day agoThe U.S. Food and Drug Administration (FDA) has ordered a software recall for a type of ventilator...
FDA approves Bristol Myers Squibb’s Breyanzi for follicular lymphoma
Pharmaceutical Technology via Yahoo Finance· 9 hours agoThe US Food and Drug Administration (FDA) has granted accelerated approval for Bristol Myers Squibb...
...What You Need to Know about FDA’s Draft Guidance on Data Integrity for In Vivo Bioavailability ...
The National Law Review· 22 hours agoGiven data integrity issues that have been uncovered in the past, in April 2024, the U.S. Food and ...
Atraverse receives approval for HOTWIRE Left Heart Access Device
Medical Device Network via Yahoo Finance· 9 hours agoAtraverse Medical has received the US Food and Drug Administration (FDA) clearance for its HOTWIRE...