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A year after FDA approves over-the-counter birth control pill, advocates push for more access
Pennsylvania Capital-Star via Yahoo News· 18 hours agoMore than 100 countries were already selling birth control without a prescription before the U.S....
FDA Roundup: May 10, 2024
Fort Wayne Journal Gazette· 1 day agoOn Thursday, the FDA provided information on how to safely charge hearing aids, glucose monitors, insulin pumps, and other medical devices to avoid overheating. Medical devices ...
No evidence Tyson Foods received FDA approval to add insects to human food | Fact check
USA TODAY via Yahoo News· 2 days agoThe claim: FDA approved use of insects in human food by Tyson Foods An April 24 Facebook post (direct link, archive link) shows the Tyson Foods logo next to an image of mealworms ...
FDA issues recall statement on insulin pump app after glitch causes more than 200 injuries
USA Today· 2 days agoThis is a Class 1 recall, which the FDA says is the most serious type of recall, and use of the...
FDA considers updating blood donation guidelines to keep nation’s supply safe from malaria
WKBT La Crosse· 2 days agoAs late as the 1940s, the US Centers for Disease Control and Prevention said Thursday in a...
Unpacking Averages: Assessing the Products Included in FDA's Voluntary Malfunction Summary Reporting...
The National Law Review· 3 days agoAt the end of 2022, FDA published a draft guidance on Voluntary Malfunction Summary Reporting (VMSR)...
FDA Finalizes Rule to Assert Authority Over Laboratory Developed Tests | JD Supra
JD Supra· 6 days agoThe Food and Drug Administration (FDA) published its long-awaited Final Rule that will regulate laboratory developed tests (LDTs) as in vitro diagnostic (IVD) medical devices ...
FDA’s Final LDT Rule Is Here, and the Changes Show the Agency Is Serious and Actually Listening to...
The National Law Review· 5 days agoThe Food and Drug Administration (FDA) published its final rule on laboratory developed tests (LDTs)...
Moderna Tumbles After The FDA Throws A Curveball On Its Second Product
Investor's Business Daily· 1 day agoThe news pushes back the potential approval of the vaccine for respiratory syncytial virus by...
JD Supra: FDA Approves New Indication for AstraZeneca and Daiichi Sankyo’s Cancer Drug ENHERTU
JD Supra· 1 day agoOn April 5, the FDA granted accelerated approval to AstraZeneca and Daiichi Sankyo’s ENHERTU (trastuzumab deruxtecan) for adult patients with unresectable or metastatic HER2 ...