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Baraka Ground Black Pepper Recalled Nationwide Due To Salmonella Risk
Real Simple· 16 hours agoThe recalled ground pepper was distributed to retail stores nationwide, and sold in 7-ounce clear plastic packages marked with an expiration date of January 2026 on the back ...
FDA urged to relax decades-old tissue donation restrictions for gay and bisexual men | Texarkana...
Texarkana Gazette· 4 days agoAdvocates, lawmakers, and groups focused on removing barriers to cornea donations, in particular,...
Philips (PHG) Boosts Precision Diagnosis With AI Platform
Zacks via Yahoo Finance· 18 hours agoThe company’s latest launch of an AI-enabled cardiovascular ultrasound platform testifies to the...
Psychedelic drug MDMA faces FDA panel in bid to become first-of-a-kind PTSD medication
FOX30 / CBS47 Jacksonville· 2 days agoThe Food and Drug Administration convened a panel of outside experts Tuesday to review the latest...
An FDA advisory committee rejected the use of MDMA to treat PTSD
Quartz· 2 days agoThe Food and Drug Administration decided to not recommend the use of the party drug MDMA, also known...
Supreme Court crunch time as Trump, abortion and social media decisions loom
USA Today· 15 hours agoThe nine justices of the Supreme Court agreed to hear 62 cases this term, which began in October....
Why is the "Right to Contraception Act" considered necessary?
NBC News via Yahoo News· 19 hours agoNebraska Gov. Jim Pillen signed a state law last year that prohibits abortion after 12 weeks of...
MDMA faces FDA panel in bid to become first-of-a-kind PTSD medication
San Jose Mercury News· 2 days agoThe Food and Drug Administration convened a panel of outside experts Tuesday to review the latest...
US FDA expands use of Bristol's cell therapy to treat rare blood cancer
Reuters· 7 days ago, opens new tab said on Thursday the U.S. FDA had allowed expanded use of its cell therapy for an...
MDMA Therapy For PTSD Closer To Legality As Key FDA Approval Meeting Approaches, Sparking Hope And...
Benzinga· 3 days agoOn Tuesday, the FDA's Psychopharmacologic Drugs Advisory Committee will meet to discuss the drug application submitted by Lykos, providing the first clear