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Nathan Reeves on Food and Drug Administration (FDA) | JD Supra
JD Supra· 5 hours agoThis Privacy Policy describes how JD Supra, LLC ("JD Supra" or "we," "us," or "our") collects, uses and shares personal data collected from visitors to ...
FDA approves Bristol Myers Squibb’s Breyanzi for follicular lymphoma
Pharmaceutical Technology via Yahoo Finance· 32 minutes agoThe US Food and Drug Administration (FDA) has granted accelerated approval for Bristol Myers Squibb...
FDA approves self-collection screening for virus that causes cervical cancer
The Day· 6 hours agoThe Food and Drug Administration this week moved to expand screening for potentially lethal cervical cancer by allowing ...
Ventilator recall issued with warning of "serious injuries or death"
Newsweek· 19 hours agoThe U.S. Food and Drug Administration (FDA) has ordered a software recall for a type of ventilator...
FDA greenlights self-collection of vaginal samples for cervical cancer screening
CNN.com· 12 hours agoInstead of a traditional speculum-involved pelvic exam to screen for cervical cancer, the US Food ...
Eisai starts rolling submission for injectable version of Alzheimer's drug with US FDA
Reuters via AOL· 1 day agoThe companies are seeking the Food and Drug Administration's (FDA) approval of a weekly dose of ...
San Diego's Cue Health had the first FDA-approved home COVID-19 test. Now the agency says to throw...
U-T San Diego· 20 hours agoThe U.S. Food and Drug Administration told consumers Monday to throw out any at-home COVID-19 tests...
IQ-AI subsidiary wins FDA designation for lead drug candidate
Proactive Investors· 6 days agoImaging Biometrics, a subsidiary of IQ-AI Ltd (LSE:IQAI, OTCQB:IQAIF), has announced that the US ...
FDA extends review of Ascendis Pharma's hypoparathyroidism drug By Investing.com
Investing.com· 2 days agoAscendis Pharma A/S (NASDAQ:ASND), a biopharmaceutical company, has received notice from the U.S. ...
US FDA declines expanded use of Dynavax's hepatitis B vaccine on insufficient data
Reuters via AOL· 2 days agoThe Food and Drug Administration in its so-called "complete response letter" stated that the data it...