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Ice cream recall update as FDA issues concern level
Newsweek· 3 days agoPreviously, the recall was not classified under any of the U.S. Food and Drug Administration's (FDA) three categories. According to the FDA website, a...
The FDA should stop letting drug companies skip steps - The Boston Globe
The Boston Globe· 3 hours agoThe FDA approves some new medical treatments quickly, before confirmatory trials are carried out, to...
RNT Health Insights’ gastric cancer detection tool receives FDA BDD
Medical Device Network via Yahoo Finance· 1 day agoThe company's flagship project targets the early detection of gastric pathologies, using a vast...
Project 2025 Has Bad Medicine for HHS
The Nation· 56 minutes agoRoger Severino, a prominent attorney for the Christian right, led the Department of Health and Human Services’ Office of Civil Rights during the Trump administration. In 2017 ...
Psychedelic Drug MDMA Faces Questions as FDA Considers Approval for PTSD
Military.com· 4 days agoFederal health regulators are questioning the safety and evidence behind the first bid to use MDMA,...
FDA warns parents to avoid infant formula distributed by Prosper company due to contamination
NBC Dallas Fort Worth· 4 days agoU.S. health officials warned parents to avoid powdered infant formula sold by a Texas dairy producer...
FDA approves Moderna’s RSV vaccine mRESVIA
Pharmaceutical Technology via Yahoo Finance· 1 day agoModerna CEO Stéphane Bancel stated: “The FDA approval of our second product, mRESVIA, builds on the strength and versatility of our mRNA platform....
FDA grants EUA for Watmind USA’s SpeedySwab Covid + FLU A&B self-test
Medical Device Network via Yahoo Finance· 1 day agoThis authorisation...well as influenzas A and B. Developed in collaboration with the National...
NIH AI tool predicts cancer patients’ immunotherapy outcomes
Pharmaceutical Technology via Yahoo Finance· 2 hours agoScientists at the US National Institutes of Health (NIH) have introduced an AI tool called Logistic...
FDA Gets Technical on HCT/P Rules in Warning Letter to Human Tissue Company | JD Supra
JD Supra· 1 day agoOn May 21, 2024, the Center for Biologics Evaluation and Research (CBER) at the U.S. Food and Drug Administration (FDA) published a warning letter issued to Akan Biosciences ...