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256 articles found
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FDA Roundup: December 10, 2024Today, the U.S. Food and Drug Administration is providing an at-a-glance summary of news from around the agency:Today, the FDA announced that, on January 1, 2025, the FDA will open the Voluntary Quali... -
FDA Roundup: December 6, 2024Today, the U.S. Food and Drug Administration is providing an at-a-glance summary of news from around the agency:On Thursday, the FDA published the draft guidance, “Expedited Program for Serious Condit...
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USDA-FDA Seek Information About Food Date Labeling, Aim is to Provide Further Clarity, Transparency and Cost Savings for U.S. ConsumersThe U.S. Food and Drug Administration (FDA) and the U.S. Department of Agriculture (USDA) today are announcing a joint Request for Information (RFI) about food date labeling, which includes the use of...
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FDA Roundup: December 3, 2024Today, the U.S. Food and Drug Administration is providing an at-a-glance summary of news from around the agency: Today, the FDA posted the final guidance on Marketing Submission Recommendations for...
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FDA Roundup: November 26, 2024Today, the U.S. Food and Drug Administration is providing an at-a-glance summary of news from around the agency: On Monday, the FDA issued this guidance: Transitional Enforcement Policy for Ethylene...
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FDA Roundup: November 22, 2024Today, the U.S. Food and Drug Administration is providing an at-a-glance summary of news from around the agency: On Thursday, the FDA published the FDA Voices: “Upholding Public Trust: FDA Office of...
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FDA Roundup: November 19, 2024Today, the U.S. Food and Drug Administration is providing an at-a-glance summary of news from around the agency: Today, the FDA issued a request for information (RFI) on per- and polyfluoroalkyl sub...
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FDA Roundup: November 15, 2024Today, the U.S. Food and Drug Administration is providing an at-a-glance summary of news from around the agency: Next week, the World Health Organization’s Member State Mechanism on Substandard and...
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FDA Approves First Gene Therapy for Treatment of Aromatic L-amino Acid Decarboxylase DeficiencyThe U.S. Food and Drug Administration approved Kebilidi (eladocagene exuparvovec-tneq), an adeno-associated virus vector-based gene therapy indicated for the treatment of adult and pediatric patients...
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FDA Roundup: November 8, 2024Today, the U.S. Food and Drug Administration is providing an at-a-glance summary of news from around the agency: Today, the FDA issued a final rule, to amend the color additive regulations to increa...