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911 articles found
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FDA Approves Three Food Colors from Natural SourcesThe U.S. Food and Drug Administration today announced it granted three new color additive petitions that will expand the palette of available colors from natural sources for manufacturers to safely us... -
FDA Announces Completion of First AI-Assisted Scientific Review Pilot and Aggressive Agency-Wide AI Rollout TimelineIn a historic first for the agency, FDA Commissioner Martin A. Makary, M.D., M.P.H., today announced an aggressive timeline to scale use of artificial intelligence (AI) internally across all FDA cente...
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FDA Announces Expanded Use of Unannounced Inspections at Foreign Manufacturing FacilitiesToday, the U.S. Food and Drug Administration announced its intent to expand the use of unannounced inspections at foreign manufacturing facilities that produce foods, essential medicines, and other me...
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HHS, FDA to Phase Out Petroleum-Based Synthetic Dyes in Nation’s Food SupplyThe U.S. Department of Health and Human Services and U.S. Food and Drug Administration (FDA) today announced a series of new measures to phase out all petroleum-based synthetic dyes from the nation’s...
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FDA Commissioner Makary Announces New Policy on Individuals Serving on FDA Advisory CommitteesIn keeping with U.S. Department of Health and Human Services Secretary Robert F. Kennedy Jr.’s promise to carry out the Department’s work with “radical transparency” and mitigate perceived industry in...
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FDA Announces Plan to Phase Out Animal Testing Requirement for Monoclonal Antibodies and Other DrugsToday, the U.S. Food and Drug Administration is taking a groundbreaking step to advance public health by replacing animal testing in the development of monoclonal antibody therapies and other drugs wi...
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Martin A. Makary, M.D., M.P.H., Sworn in as FDA CommissionerRenowned surgeon-scientist and health policy expert, Martin A. Makary, M.D., M.P.H., took the oath of office to become the 27th Commissioner of Food and Drugs. Dr. Makary was confirmed by a bipartisan...
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FDA Roundup: March 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’s Learning and Education to ADvance and Empower Rare Disease Drug D...
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FDA Grants Marketing Authorization of First Home Test for Chlamydia, Gonorrhea and TrichomoniasisToday, the U.S. Food and Drug Administration granted marketing authorization to Visby Medical for the Visby Medical Women’s Sexual Health Test. This is the first diagnostic test for chlamydia, gonorrh...
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FDA Roundup: March 21, 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 Fabhalta (iptacopan) for the treatment of adults with comp...