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FDA Drug Safety Podcasts
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268
FDA
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Coronavirus (COVID-19) Update: FDA Limits Use of Certain Monoclonal Antibodies to Treat COVID-19 Due to the Omicron Variant
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278
FDA
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Increase in manufacturing capacity for Vaxzevria (previously COVID-19 Vaccine AstraZeneca), CHMP, 24/01/2022
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287
EMA
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International regulators’ recommendations on COVID-19 vaccines and the Omicron variant, , 21/01/2022
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473
EMA
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Meeting highlights from the Committee for Medicinal Products for Veterinary Use (CVMP) 18-19 January 2022, CVMP, 21/01/2022
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331
EMA
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Office of Prescription Drug Promotion (OPDP) Metrics
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259
FDA
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Technical Specifications for Submitting Clinical Trial Data Sets for Treatment of Noncirrhotic Nonalcoholic Steatohepatitis (NASH)
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368
FDA
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Collecting and Providing 702(b) Portions of FDA Official Samples
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243
FDA
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FDA Public Meeting: Identification of Concepts and Terminology for Multi-Component Biomarkers - 03/23/2022
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288
FDA
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FDA Takes Actions to Expand Use of Treatment for Outpatients with Mild-to-Moderate COVID-19
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328
FDA
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Alma LeVant Hayden's Contributions to Regulatory Science
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248
FDA
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Summary of Color Additives for Use in the United States in Foods, Drugs, Cosmetics, and Medical Devices
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371
FDA
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From Our Perspective
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291
FDA
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Mylan Pharmaceuticals Inc., a Viatris Company, Conducting Voluntary Recall of One Batch of Semglee® (insulin glargine injection), 100 units/mL (U-100)
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507
FDA
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Summitt Labs Issues Voluntary Nationwide Recall of KORE ORGANIC Watermelon CBD Oil Due to High Lead Results
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373
FDA
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Durisan Hand Sanitizer Recall Due to Microbial Contamination
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256
FDA
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Drug Supply Chain Security Act Law and Policies
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253
FDA
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Acella Pharmaceuticals, LLC Issues Voluntary Nationwide Recall of Certain Lots of NP Thyroid® (Thyroid Tablets, USP) Due to Super Potency
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385
FDA
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Fat Burners Zone Issues Voluntary Nationwide Recall of Zero Xtreme Due to Presence of Undeclared Sibutramine
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297
FDA
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Orange Book Preface
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319
FDA
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