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FDA lifts partial clinical hold on Larimar’s Friedreich’s ataxia treatment
Endpoints News· 5 days agoLarimar Therapeutics’ stock $LRMR shot up by as much as 20% after announcing Monday that the FDA had...
LDTs: FDA Rolls Out a Phased Implementation for New Regulatory Requirements
The National Law Review· 6 days agoOn May 6, 2024, the U.S. Food and Drug Administration (FDA) issued its final rule significantly...
Nearly 1.9 million cases of water impacted by FDA recall
KSNT Topeka· 10 hours agoThe Food and Drug Administration (FDA) says a bottled water producer is recalling thousands of cases...
FDA Roundup: May 24, 2024
The Woonsocket Call· 1 day agoOn Thursday, the FDA announced that Medline Industries, LP, a firm marketing and distributing plastic syringes made in China within the U.S., initiated a recall to stop using ...
Guardant Health Jumps — As Exact Sciences Slumps — On A Key FDA Move For Blood Tests
Investor's Business Daily· 1 day agoGuardant Health stock jumped Friday after a Food and Drug Administration panel recommended the...
It’s Official: Tara Flour Is an Unapproved Food Additive, According to the FDA
Eating Well via Yahoo News· 4 days agoTara flour made headlines in 2022 after hundreds got sick from Daily Harvest crumbles. Now the FDA...
FDA panel backs Guardant’s blood test for colon cancer
MedTech Dive via Yahoo Finance· 2 days agoWilliam Blair analyst Andrew Brackmann said the FDA appears on its way to approving Shield. Still,...
Blood test that detects colon cancer close to receiving FDA approval
News 12· 5 hours agoA blood test that detects colon cancer is one step closer to being approved by the Food and Drug Administration. The Guardant Shield blood test has been available for two years and costs $900 ...
FDA grants IND clearance for Abdera’s Phase I cancer therapy trial
Clinical Trials Arena via Yahoo Finance· 2 days agoThe US Food and Drug Administration (FDA) has granted clearance for Abdera Therapeutics'...
Breaking: FDA authorizes second patient for Elon Musk's Neuralink brain chip trial | Invezz
Invezz· 6 days agoThe United States Food and Drug Administration (FDA) has authorized a second patient for Neuralink’s...