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HIV and Hepatitis: Know Your Status and Learn About the FDA's Role
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276
FDA
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Prescription Stimulant Medications
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237
FDA
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Paving the way towards coordinated clinical trials in public health emergencies in the EU, , 25/07/2023
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296
EMA
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CytoDyn, Inc. - 626957 - 02/11/2022
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243
FDA
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CytoDyn, Inc. - 626957 - 04/27/2023
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221
FDA
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Advancing Real-World Evidence Program Frequently Asked Questions
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205
FDA
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Guidance for Industry | M7(R2) Assessment and Control of DNA Reactive (Mutagenic) Impurities in Pharmaceuticals To Limit Potential Carcinogenic Risk
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223
FDA
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Wise Women’s Choice - 658897 - 07/20/2023
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433
FDA
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Online Controlled Substances Summits
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279
FDA
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Counterfeit Medicine
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221
FDA
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Gadget Island, Inc. - 658733 - 07/21/2023
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261
FDA
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FDA Roundup: July 25, 2023
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249
FDA
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Questions and Answers | M7(R2) Assessment and Control of DNA Reactive (Mutagenic) Impurities in Pharmaceuticals To Limit Potential Carcinogenic Risk
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304
FDA
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M7(R2) ADDENDUM: APPLICATION OF THE PRINCIPLES OF THE ICH M7 GUIDELINE TO CALCULATION OF COMPOUND-SPECIFIC ACCEPTABLE INTAKES
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240
FDA
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M7(R2) Assessment and Control of DNA Reactive (Mutagenic) Impurities in Pharmaceuticals To Limit Potential Carcinogenic Risk—Questions and Answers
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368
FDA
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Advancing Generic Drug Development: Translating Science to Approval 2023 - 09/13/2023
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197
FDA
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OTC Monograph Reform: OMOR Format and Content & Electronic Submissions - 08/22/2023
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235
FDA
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M7(R2) Assessment and Control of DNA Reactive (Mutagenic) Impurities in Pharmaceuticals To Limit Potential Carcinogenic Risk
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Views
260
FDA
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First RSV vaccine to protect infants up to 6 months of age and older adults, CHMP, 21/07/2023
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287
EMA
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Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 17-20 July 2023, CHMP, 21/07/2023
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303
EMA
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