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Document: List of European Union reference dates (EURD) and frequency of submission of periodic safety update reports (PSURs)-2025/5/28
2025-05-29查看详情 > -
Document: Start of procedure - extension of marketing authorisation (26 April - 22 May 2025)-2025/5/27
2025-05-28查看详情 > -
Document: Start of procedure: Type II variation - extension of indication (26 April - 22 May 2025)-2025/5/27
2025-05-28查看详情 > -
Document: Minutes of the CHMP meeting 9-12 December 2024-2025/5/27
2025-05-28查看详情 > -
Document: Overview of (invented) names reviewed in April 2025 by the Name Review Group (NRG) adopted at the CHMP meeting of 22 May 2025-2025/5/27
2025-05-28查看详情 > -
Document: CTIS newsflash - 27 May 2025-2025/5/27
2025-05-28查看详情 > -
Document: List of centrally authorised products with safety-related changes to the product information-2025/5/27
2025-05-28查看详情 > -
Document: Pharmacovigilance-related regulatory recommendations for centrally authorised veterinary medicinal products during 2025-2025/5/27
2025-05-28查看详情 > -
Page: EudraVigilance training and support-2025/5/27
2025-05-28查看详情 > -
Page: Quality of medicines questions and answers: Part 1-2025/5/27
2025-05-28查看详情 >