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Regulatory and procedural guideline: Compilation of Union procedures on inspections and exchange of information-2023/7/13
2023-07-21查看详情 > -
Page: Evaluation of medicinal products indicated for treatment of bacterial infections - Scientific guideline-2024/2/9
2024-03-11查看详情 > -
Document: Draft reflection paper on the qualification of non-mutagenic impurities-2025/1/30
2025-02-05查看详情 > -
Document: Minutes of the CHMP meeting on 14-17 October 2024-2025/3/7
2025-03-10查看详情 > -
Document: List of medicines currently in PRIME scheme-2025/4/9
2025-04-11查看详情 > -
Document: Orientation guide for delegates - EMA building-2025/5/22
2025-05-23查看详情 > -
Document: List of changes to combined Veterinary Dictionary for Drug Regulatory Activities (VeDDRA) list of clinical terms for reporting suspected adverse events in animal and humans to veterinary medicinal products for 2024-2025/6/27
2025-06-30查看详情 > -
Document: List of medicinal products under additional monitoring-2025/7/30
2025-07-31查看详情 > -
Document: Questions and answers on Implementing Regulation (EU) 2025/1466: Amendment of Regulation (EU) No 520/2012 and Conclusion of the Signal Detection in EudraVigilance Pilot by marketing authorisation holders-2025/9/17
2025-09-18查看详情 > -
Document: Clinical Trial Information System (CTIS) structured data form - Notifications, Annual Safety Report (ASR) and results-2025/10/23
2025-10-24查看详情 >