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At FDA, full vaccine approval is the gold standard. The agency was on track to sign off on Novavax’s license by its April 1 ...
Comments over the weekend by FDA chief Martin Makary suggest the agency views Novavax’s updated COVID shot as a “new product” ...
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Pharmaceutical Technology on MSNFDA layoffs and priority review programme’s lapse disrupt rare disease pipelineThe expiration of the FDA’s paediatric priority review voucher programme is creating uncertainty for rare disease drug ...
Avant Technologies, Inc. (OTCQB: AVAI) ("Avant" or the "Company"), and its JV partner, Ainnova Tech, Inc., (Ainnova), a leading healthcare technology company focused on revolutionizing early disease ...
On a recent call with analysts at BMO Capital Markets, a “former director” at the FDA’s Center for Biologics Evaluation and ...
When detox timing is a concern, the TestClear Powdered Urine Kit provides a guaranteed way to pass a urine drug test. Unlike ...
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The Manila Times on MSNAqua Sculpt Reviews Consumer Reports (BREAKING) Shocking Complaints And Honest Customer Reviews Reported!Overall, complaints are relatively rare compared to positive reviews, and the company offers a 180-day money-back guarantee ...
AstraZeneca has axed three MedImmune legacy monoclonal antibody drugs from its neuroscience pipeline in a first-quarter clear ...
The potential dangers of these food dyes have been spoken about for years. Here's everything parents need to know.
Medical device maker ICU Medical changed the designs of infusion pumps made in Minnesota without properly clearing important ...
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News-Medical.Net on MSNMursla Bio receives FDA breakthrough device designation for EvoLiver testMursla Bio, a leader in Extracellular Vesicle (EV) science on a mission to significantly improve cancer outcomes for at-risk ...
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