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FDA "inadvertently archived" complaint about infant formula
CBS News via Yahoo News· 17 hours ago"More could have been done leading up to the Abbott powdered infant formula recall," noted the...
FDA elevates Medline recall of endotracheal ventilator tubes
FierceBiotech· 2 days agoThe company’s SubG ventilation tubes deliver oxygen down the throat and into the patient’s lungs and...
Client Alert: Access to Mifepristone Still Standing for Now, but Questions Remain | JD Supra
JD Supra· 1 day agoOn Thursday morning, the Supreme Court issued its decision in FDA v. Alliance for Hippocratic Medicine. Justice Kavanaugh wrote for a unanimous Court...lack of Article III ...
Unanimous Supreme Court Finds No Standing to Challenge FDA Regulation of Mifepristone (UPDATED)
Reason.com· 2 days agoFood & Drug Administration. Justice Thomas also wrote a separate concurrence on third-party and associational standing. As I documented in a series of posts (linked here and ...
Concern Grows Over Bird Flu Outbreak in Dairy Cows
The Dispatch via Yahoo News· 24 hours ago“The plaintiffs may present their concerns and objections to the President and FDA in the regulatory process, or to Congress and the President in the...
SCOTUS Just Made a Final Decision About Abortion Pill Access
Cosmopolitan via AOL· 2 days agoA reminder first: What exactly are abortion pills? Great question. In 2000, the FDA approved this...
FDA panel approves Alzheimer's drug that can slow disease
KTVB Boise· 5 days ago“I thought the evidence was very strong in the trial showing the effectiveness of the drug,” said...
Why FDA Panel Rejected MDMA Therapy—And What’s Next For Psychedelic Medicine
Forbes· 2 days agoHigh hopes that psychedelic medicines were finally on the pathway to regulation were dashed last...
Supreme Court Rejects Abortion Pill Challenge, Preserving Wide Access to Drug
The Wall Street Journal· 2 days agoThe court ruled that a group of antiabortion doctors who filed suit had no legal standing to...
Co-Diagnostics Submits At-Home PCR System, COVID-19 Test to FDA
GenomeWeb News· 18 hours agoCo-Diagnostics announced on Friday that it has submitted a PCR instrument and COVID-19 test to the US Food and Drug Administration for 510(k) clearance. The firm has submitted the system for ...