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No evidence Tyson Foods received FDA approval to add insects to human food | Fact check
USA TODAY via Yahoo News· 1 day 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 ...
One year after FDA approves over-the-counter birth control pill, advocates push for more access
NC Newsline via Yahoo News· 16 hours ago“My parents are immigrants from India, and it’s been over the counter there since my mom can...
A New Oral Antibiotic Is Available to Treat UTIs
Verywell Health via Yahoo News· 3 days agoIllustration by Zoe Hansen for Verywell Health Fact checked by Nick Blackmer Key Takeaways The FDA approved a new oral antibiotic called Pivya to treat...
FDA To Hold Advisory Committee Meeting On MDMA Therapy For PTSD, Welcomes Public Comment
Forbes· 21 hours agoThe U.S. Food and Drug Administration (FDA) recently announced an upcoming committee meeting...
JD Supra: FDA Approves New Indication for AstraZeneca and Daiichi Sankyo’s Cancer Drug ENHERTU
JD Supra· 1 day agoENHERTU, which is now FDA-approved for five indications, is a specifically engineered HER2-directed antibody drug conjugate (“ADC”) discovered by Daiichi ...
Eli Lilly Alzheimer’s drug gets FDA panel date after approval delay
The Hill via AOL· 4 days agoAn outside panel of advisers to the Food and Drug Administration (FDA) will meet next month to...
FDA Approves Azurity Pharmaceuticals’ Myhibbin as an Oral Suspension for Organ Transplant Recipients
Pharmaceutical Executive Magazine· 5 days agoAxurity Pharmaceuticals announced that the FDA has officially approved Myhibbin as a ready-to-use...
FDA Finalizes Rule to Assert Authority Over Laboratory Developed Tests | JD Supra
JD Supra· 6 days agoRule that will regulate laboratory developed tests (LDTs) as in vitro diagnostic (IVD) medical devices. FDA published a four-year enforcement discretion phaseout plan as part ...
FDA delays decision on Moderna RSV vaccine
BioPharma Dive via Yahoo Finance· 2 days agoThe regulator cited “administrative constraints,” rather than any issue with Moderna’s trial data, for missing a May 12 deadline, the company said.
FDA approves CereVasc’s eShunt system study for hydrocephalus
Medical Device Network via Yahoo Finance· 4 days agoIn June 2023, CereVasc partnered with LianMedical to introduce its eShunt System and related...
