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911 articles found
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HHS, FDA Announce Operation Stork Speed to Expand Options for Safe, Reliable, and Nutritious Infant Formula for American FamiliesToday, under the leadership of U.S. Department of Health and Human Services Secretary Robert F. Kennedy, Jr., the U.S. Food and Drug Administration is taking steps to enhance its efforts to ensure the... -
FDA Roundup: March 18, 2025Today, the U.S. Food and Drug Administration is providing an at-a-glance summary of news from around the agency:On Tuesday, March 18, the United States District Court for the District of Maryland ente...
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FDA Educational Efforts Prevented Nearly 450,000 Youth from Starting E-Cigarette Use in One YearToday, a study co-authored by U.S. Food and Drug Administration scientists was released showing the agency’s youth e-cigarette prevention campaign, “The Real Cost,” successfully reduced e-cigarette us...
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FDA Roundup: March 14, 2025Today, the U.S. Food and Drug Administration is providing an at-a-glance summary of news from around the agency:On Thursday, the FDA posted information on the flu vaccine composition for the 2025-2026...
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FDA Roundup: March 11, 2025Today, the U.S. Food and Drug Administration is providing an at-a-glance summary of news from around the agency:Today, the FDA published a General Correspondence Letter issued to Mid-Link Technology T...
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FDA Roundup: March 7, 2025Today, the U.S. Food and Drug Administration is providing an at-a-glance summary of news from around the agency:On Wednesday, the FDA approved Encelto (revakinagene taroretcel-lwey), an allogeneic enc...
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FDA Roundup: February 28, 2025Today, the U.S. Food and Drug Administration is providing an at-a-glance summary of news from around the agency:On Thursday, the FDA approved Odactra to include use in individuals 5 through 11 years o...
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FDA Approves First Treatment for Cerebrotendinous Xanthomatosis, a Rare Lipid Storage DiseaseToday, the U.S. Food and Drug Administration approved Ctexli (chenodiol) for the treatment of cerebrotendinous xanthomatosis (CTX) in adults. Ctexli is the first FDA-approved drug to treat CTX, a very...
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FDA Approves First Rapid-Acting Insulin Biosimilar Product for Treatment of DiabetesToday, the U.S. Food and Drug Administration approved Merilog (insulin-aspart-szjj) as biosimilar to Novolog (insulin aspart) for the improvement of glycemic control in adults and pediatric patients w...
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FDA Alerts Patients of Potential to Miss Critical Safety Alerts Due to Phone Settings When Using Smartphone-Compatible Diabetes DevicesToday, the U.S. Food and Drug Administration is alerting patients of a safety concern regarding diabetes devices, such as continuous glucose monitors (CGMs), insulin pumps and automated insulin dosing...