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911 articles found
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Coronavirus (COVID-19) Update: FDA Recommends Inclusion of Omicron BA.4/5 Component for COVID-19 Vaccine Booster DosesOn Tuesday, the U.S. Food and Drug Administration’s independent experts on the Vaccines and Related Biological Products Advisory Committee met to publicly discuss whether a change to the current vacci... -
FDA Infant Formula Update: June 30, 2022Today, the U.S. Food and Drug Administration is providing an update on additional steps it has taken that will lead to more infant formula available in the U.S. under the agency’s recent increased fle...
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FDA Roundup: June 28, 2022Today, the U.S. Food and Drug Administration is providing an at-a-glance summary of news from around the agency: Today, the FDA and HHS/ASPR announced the authorization of an extension to the shelf-l...
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FDA Infant Formula Update: June 28, 2022Today, the U.S. Food and Drug Administration is providing an update on additional steps it has taken that will lead to more infant formula available in the U.S. under the agency’s recent increased fle...
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FDA Introduces Innovative Proposal to Advance Consumer Access to Nonprescription DrugsToday, the U.S. Food and Drug Administration issued a proposed rule titled, “Nonprescription Drug Product with an Additional Condition for Nonprescription Use,” which is intended to broaden the range...
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FDA Infant Formula Update: June 27, 2022Today, the U.S. Food and Drug Administration is providing an update on additional steps it has taken that will lead to more infant formula available in the U.S. under the agency’s recent increased fle...
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FDA Roundup: June 24, 2022Today, the U.S. Food and Drug Administration is providing an at-a-glance summary of news from around the agency: Today, the FDA announced its recognition of JANAAC as an Accreditation Body Under FSMA...
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FDA Releases Action Plan for Rare Neurodegenerative Diseases, Including ALSToday, the U.S. Food and Drug Administration unveiled its Action Plan for Rare Neurodegenerative Diseases including Amyotrophic Lateral Sclerosis (ALS) – a five-year strategy for improving and extendi...
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FDA Denies Authorization to Market JUUL ProductsToday, the U.S. Food and Drug Administration issued marketing denial orders (MDOs) to JUUL Labs Inc. for all of their products currently marketed in the United States. As a result, the company must st...
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FDA Infant Formula Update: June 22, 2022Today, the U.S. Food and Drug Administration is providing an update on additional steps it has taken that will lead to more infant formula available in the U.S. under the agency’s recent increased fle...