A clinical trial comparing a one-page medication handout proposed by the U.S. Food and Drug Administration (FDA) with an ...
The drugmaker expects the regulator to remove Wegovy and Ozempic from its shortage list, blocking other companies from ...
The U.S. Food and Drug Administration has labeled the broccoli recall as a Class I, the highest risk level issued by the agency.
The U.S. Food and Drug Administration approved a new non-opioid pain medication developed by the Massachusetts-based company ...
Going forward, we may see more instances in which insurers deny or (temporarily) severely restrict coverage of accelerated ...
Robert Califf addressed a range of issues, including AI, lack of nutrition resources at the FDA and how he evaluates the progress of precision medicine at the Precision Medicine World Conference in ...
Broccoli sold at Walmart in 20 states has been labeled potentially deadly in an update from the FDA. Was it sold in ...
The FDA will allow two biotechnology companies to run clinical trials: United Therapeutics and eGenesis. United Therapeutics ...
These risks prompted California to ban its use in food in 2023 and the Food and Drug Administration to ban its use in ...
(Scott Olson/Getty Images) In the final days of the Biden administration, the Food and Drug Administration proposed ... including the FDA and the Centers for Disease Control and Prevention ...
The U.S. Food and Drug Administration has approved Axsome Therapeutics' migraine treatment, the company said on Thursday.
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Hosted on MSNFDA grants orphan drug status to Arbor Biotechnologies’ PH1The US Food and Drug Administration (FDA) has granted orphan drug designation (ODD) and rare paediatric disease designation (RPDD) to Arbor Biotechnologies' gene editing therapeutic, ABO-101, to treat ...
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