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Document: Minutes of the PRAC meeting 25-28 November 2024-2025/4/9
2025-04-11查看详情 > -
Page: COVID-19 vaccines: key facts-2025/5/21
2025-05-22查看详情 > -
Document: Call for comments on the Veterinary Dictionary for Drug Regulatory Activities (VeDDRA) standard list for EudraVigilance Veterinary (EVVet)-2025/6/27
2025-06-30查看详情 > -
Page: Emtricitabine/tenofovir disoproxil product-specific bioequivalence guidance-2025/7/30
2025-07-31查看详情 > -
Document: UPD registration guide for UI and API users-2025/9/17
2025-09-18查看详情 > -
Document: Overview of (invented) names reviewed in September 2025 by the Name Review Group (NRG) adopted at the CHMP meeting of 16 October 2025-2025/10/23
2025-10-24查看详情 > -
Document: Meeting report - EMA workshop on the challenges in drug development, regulation and clinical practice for immunoglobulins-2025/11/25
2025-11-26查看详情 > -
Document: Table of decisions of labelling exemption requests falling under article 63 of Directive 2001/83/EC examined by the Quality Review of Documents (QRD) Group-2025/12/17
2025-12-18查看详情 > -
Document: Frequently asked questions on the European Shortages Monitoring Platform (ESMP)-2026/2/2
2026-02-03查看详情 > -
关于公开征求《罕见病酶替代疗法药物药学研究与评价技术指导原则（征求意见稿）》意见的通知-2026/3/11
2026-03-12查看详情 >
