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NCTR Annual Reports
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301
FDA
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International regulators and WHO: support healthcare professionals to enhance public confidence in COVID-19 vaccines, , 17/05/2022
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264
EMA
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Drug Approval Case Studies
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251
FDA
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Assessing User Fees Under the Generic Drug User Fee Amendments of 2017
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212
FDA
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Specialty Process Labs LLC - 624281 - 05/03/2022
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317
FDA
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Colorful Products Corporation - 624415 - 05/10/2022
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252
FDA
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FDA Seeks to Engage Stakeholders on Key Considerations for a Drug Quality Management Maturity Program
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252
FDA
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Drug Trials Snapshots
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275
FDA
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President's Emergency Plan for AIDS Relief (PEPFAR)
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306
FDA
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Gerrit Johan Schefferlie elected new Chair of EMA Committee for Veterinary Medicinal Products (CVMP), CVMP, 13/05/2022
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259
EMA
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FDA Patient Engagement Partnerships
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284
FDA
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Investigating Out-of-Specification (OOS) Test Results for Pharmaceutical Production - Level 2 revision
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293
FDA
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Meeting highlights from the Committee for Veterinary Medicinal Products (CVMP) 10-12 May 2022, CVMP, 13/05/2022
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270
EMA
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Gerrit Johan Schefferlie elected new Chair of EMA Committee for Medicinal Products for Veterinary Use (CVMP), CVMP, 13/05/2022
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275
EMA
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Pediatric Tracking Requirements Under FDAAA
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259
FDA
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CDER Launches New Accelerating Rare disease Cures (ARC) Program
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252
FDA
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FDA Approves Oral Form for the treatment of adults with amyotrophic lateral sclerosis (ALS)
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250
FDA
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Azurity Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of One Lot of Firvanq® (Vancomycin Hydrochloride for Oral Solution), Vancomycin 50 mg
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395
FDA
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From Our Perspective: FDA’s Role in Helping a Critical Medical Isotope Meet Sufficient Supply in the US for First Time
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429
FDA
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The Collection | From Our Perspective
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310
FDA
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