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Patient Materials
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390
FDA
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2018-NCTR Research Highlights
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320
FDA
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Voluntary Recall of Certain Colgate Products Sold at Family Dollar Stores Because They Were Stored Outside of Temperature Requirements
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364
FDA
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Developing a Toolkit to Assess Efficacy of Ebola Vaccines and Therapeutics
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304
FDA
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Most Recent Changes to the IID Database
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308
FDA
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A Recipe for Danger: Social Media Challenges Involving Medicines
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232
FDA
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Instructions for Completing Form FDA 3500
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290
FDA
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MedWatch Forms for FDA Safety Reporting
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349
FDA
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Q&A on CGMP Requirements
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363
FDA
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Questions and Answers on Current Good Manufacturing Practice Questions and Answers on Current Good Manufacturing Practice Requirements | General Provi
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343
FDA
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Educational Resources
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224
FDA
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FDA and NIH Launch Public-Private Partnership for Rare Neurodegenerative Diseases
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278
FDA
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2020 Meeting Materials, Nonprescription Drugs Advisory Committee
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235
FDA
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2019 Meeting Materials, Nonprescription Drugs Advisory Committee
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237
FDA
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Adapted vaccine targeting BA.4 and BA.5 Omicron variants and original SARS-CoV-2 recommended for approval, CHMP, 12/09/2022
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256
EMA
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Amneal Pharmaceuticals Issues Voluntary Nationwide Recall of Lorazepam Oral Concentrate, USP 2mg/mL, Due to Misprinted Dosing Droppers Supplied with t
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264
FDA
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MPM Medical LLC Issues Voluntary Nationwide Recall of Regenecare HA Hydrogel Due to Burkholderia cepecia Contamination
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362
FDA
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Fresenius Kabi Issues Voluntary Nationwide Recall of a Single Lot of Dexmedetomidine Hydrochloride Injection Due to Cross-Contamination of Lidocaine
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266
FDA
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Fresenius Kabi Issues Voluntary Nationwide Recall of Two Lots of Dexmedetomidine Hydrochloride Injection Due to Cross-Contamination of Lidocaine
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302
FDA
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Dermatologic and Ophthalmic Drugs Advisory Committee Roster
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275
FDA
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