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San Diego COVID-19 testmaker Cue Health is shutting down
U-T San Diego· 9 minutes agoThe San Diego firm said it has stopped selling the COVID-19 tests, which was its only fully FDA...
US FDA staff says Guardant's test may fail to detect some pre-cancerous tumors
Reuters via Yahoo News· 7 hours agoThe reviewers, however, said the test may increase compliance with screening for colorectal cancer...
As Florida opens new paths to psychedelic therapy, treatment must be available to all | Opinion
Miami Herald via Yahoo News· 1 minute agoPsychedelic and empathogenic compounds have only recently gained traction in a medical setting, but MDMA was originally invented in 1912, and psilocybin, the active compound in “magic mushrooms ...
Check Your Pantry: Over 30 Pretzel Products Recalled Nationwide Due to Salmonella Risk
Martha Stewart Living via Yahoo News· 6 hours agoThis recall is an expansion on a May 6 recall involving products from Palmer Candy Company,...
Larimar Therapeutics' Friedreich's Ataxia Investigational Drug Differentiated From Biogen's Marketed...
Benzinga· 2 hours agoLarimar Therapeutics announces FDA lift of partial clinical hold on nomlabofusp (CTI-1601) for...
FDA allows Neuralink to implant 2nd patient with brain chip
FOX 10 Phoenix· 45 minutes agoThe Food and Drug Administration has approved Neuralink to implant its brain chip into a second...
FDA sets new review date for Halozyme's drug delivery tech By Investing.com
Investing.com· 3 hours agoHalozyme (NASDAQ:HALO) Therapeutics, Inc. (NASDAQ: HALO) announced that the U.S. Food and Drug...
LDTs: FDA Rolls Out a Phased Implementation for New Regulatory Requirements | JD Supra
JD Supra· 13 hours agoOn May 6, 2024, the U.S. Food and Drug Administration (FDA) issued its final rule significantly modifying FDA’s approach to oversight of laboratory developed ...
FDA Finalizes Rule and Sets Course to Phase In Oversight of Laboratory Developed Tests | JD Supra
JD Supra· 13 hours agoOn May 6, 2024, following more than a decade of discourse with interested stakeholders on potential approaches to regulation of laboratory developed tests (LDTs), the U.S. Food and Drug Administration ...
Roche Breast Cancer Medicine to Get Expedited FDA Review
Bloomberg· 10 hours agoRoche Holding AG said an experimental breast-cancer treatment will get an expedited review from US...