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Axogen begins FDA submission for nerve graft product By Investing.com
Investing.com· 12 hours agoAxogen, Inc. (NASDAQ: AXGN), a company specializing in surgical solutions for peripheral nerve...
US unveils proposal to ease restrictions on marijuana
Reuters via Yahoo News· 7 hours agoThe U.S. Justice Department on Thursday unveiled a historic proposal to ease restrictions on...
FDA extends review of Ascendis Pharma's hypoparathyroidism drug By Investing.com
Investing.com· 2 days agoAscendis Pharma A/S (NASDAQ:ASND), a biopharmaceutical company, has received notice from the U.S. ...
Eisai starts rolling submission for injectable version of Alzheimer's drug with US FDA
Reuters via AOL· 2 days agoThe companies are seeking the Food and Drug Administration's (FDA) approval of a weekly dose of ...
Imported Drugs: (Possibly) Coming Soon to a State Near You
The National Law Review· 5 hours agoAs we previously discussed, the US Department of Health and Human Services (HHS) issued a final rule...
FDA greenlights self-collection of vaginal samples for cervical cancer screening
CNN.com· 1 day agoInstead of a traditional speculum-involved pelvic exam to screen for cervical cancer, the US Food ...
Eisai initiates rolling Biologics License Application to US FDA for Leqembi® (lecanemab-irmb) for...
FOX 23 News Albany· 2 days agoFood and Drug Administration (FDA) for lecanemab-irmb (U.S. brand name: Leqembi) subcutaneous...
Getinge to limit US sales of heart devices after FDA safety warning
MedTech Dive via Yahoo Finance· 14 hours ago“It is related to working through the challenges on the balloon pump itself. There's some technical ...
Diasorin Nabs FDA 510(k) Clearance for Expanded Respiratory Panel
GenomeWeb News· 4 hours agoDiasorin said on Thursday that the US Food and Drug Administration has granted 510(k) marketing clearance for an updated ...
Wondfo USA’s Covid-19/Influenza Test receives FDA EUA approval
Medical Device Network via Yahoo Finance· 16 hours agoA&B Test received emergency use authorisation (EUA) from the US Food and Drug Administration (FDA
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