The U.S. Food and Drug Administration approved Merilog as biosimilar to Novolog for the improvement of glycemic control in adults and pediatric ...
Penn State Extension will offer a course to help produce growers meet food safety rules as outlined in the Food Safety Modernization Act, also known as FSMA, administered by the U.S. Food and Drug ...
Dr. Jacqueline Corrigan-Curay, acting director of the FDA's Center for Drug Evaluation and Research, said the approval offers an opportunity to mitigate certain risks associated with using an ...
In this regard, CPS has written a letter to all the state medical councils requesting them to send a copy of the certificates of the students coming for additional qualification to CPS for ...
The FDA has assigned a Prescription Drug User Fee Act (PDUFA) target action date of September 14, 2025. This NDA acceptance represents a pivotal milestone for Corstasis Therapeutics, signifying the ...
The nasal spray Spravato, which is made from the drug esketamine ... it had to be used in conjunction with an oral medication. The FDA has now expanded its approval to include the standalone ...
Clinical trials of the first drugs designed with the help of artificial intelligence could commence this year, Google DeepMind CEO Demis Hassabis suggested Tuesday. Speaking on a panel at the World ...
The U.S. Food and Drug Administration expanded approval for Johnson & Johnson’s nasal spray, Spravato, to allow it to be used as a standalone treatment for patients with severe depression ...
The decision builds on previous FDA approval for the drug’s treatment when combined with additional oral antidepressants. While Spravato’s underlying mechanisms remain unclear and only be ...
Cortland, New York – Cortland Biomedical, a full-service biomedical textile product development partner that provides access to a full spectrum of global engineering, design, and manufacturing ...
21 (UPI) --The Food and Drug Administration has approved the first ... response to at least two oral antidepressants, the FDA announced Tuesday. Advertisement MDD is one of the most common ...
The FDA is reviewing new vaccines for meningitis and chikungunya and therapies for Parkinson disease and PTSD. The FDA is reviewing the resubmitted NDA for SPN-830, an apomorphine infusion device for ...
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