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5 takeaways from Fauci’s heated House hearing
The Hill· 3 hours agoDuring his first congressional hearing in nearly two years, former chief White House medical adviser Anthony Fauci picked up where he left off: trading...
FDA warns parents to avoid infant formula distributed by Texas company due to contamination
WWTI Watertown· 3 days agoWASHINGTON (AP) — U.S. health officials warned parents to avoid powdered infant formula sold by a...
Fentanyl vs Dilaudid: Which Is Better?
Verywell Health via Yahoo News· 6 hours agoIn 2022, illegal fentanyl products were responsible for 70% of deaths due to drug overdoses in the U.S. Over 76,000 people died from fentanyl overdoses...
Is Pfizer Inc. (NYSE:PFE) the Best Gene Therapy Stock to Buy Now?
Insider Monkey via Yahoo Finance· 4 hours agoWe recently compiled a list of the 9 Best Gene Therapy Stocks to Buy Now and in this article, we...
FDA responds to senator’s letter that calls out ‘FDA’s failure to act’ on NOW’s test results
Nutraingredients.com· 3 days agoLast April, South Carolina Congressman Jeff Duncan wrote to FDA Commissioner Dr. Robert Califf,...
FDA Roundup: May 28, 2024
WKBN 27 Youngstown· 6 days agoOn Friday, the FDA announced it had opened a new period for applications for grants to support the development and potential approval or conditional approval of new animal ...
FDA staff questions safety of ecstasy for PTSD
Axios· 3 days agoWhy it matters: The findings cast new doubts on what could become the first psychedelic-based treatment approved in the U.S. ahead of a June 4 meeting...
FDA finalizes guidance on “Remanufacturing” vs “Servicing” | JD Supra
JD Supra· 5 days agoIn June 2021, FDA issued draft guidance on “Remanufacturing of Medical Devices,” aiming to help clarify the point when manipulation or repair of a medical device becomes “ ...
The FDA is weighing whether to approve MDMA for PTSD. Here's what that could look like for patients.
CBS News· 3 days agoDetails of the FDA's proposal were published Friday in a set of documents released by the agency...
FDA Approves First Interchangeable Biosimilar for Two Rare Diseases
WROC Rochester· 6 days agoToday, the U.S. Food and Drug Administration approved Bkemv (eculizumab-aeeb) as the first interchangeable biosimilar to Soliris (eculizumab) to treat certain rare diseases. "Many rare conditions ...