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Document: Guidance for Rapporteurs and members of drafting groups of documents developed by the GMP/GDP Inspectors Working Group-2025/3/27
2025-03-28查看详情 > -
Page: SME Regulation and reports-2025/5/2
2025-05-06查看详情 > -
Document: List of metadata for the HMA-EMA Catalogues of real-world data sources and studies-2025/6/12
2025-06-13查看详情 > -
Page: Paediatric investigation plans: questions and answers-2025/7/17
2025-07-18查看详情 > -
Page: Administration and Corporate Management-2025/9/1
2025-09-02查看详情 > -
Document: Timetable: Companion diagnostic follow-up consultation - ATMP-2025/10/3
2025-10-08查看详情 > -
关于公开征求《中药提取物质量控制研究技术指导原则（征求意见稿）》意见的通知-2025/11/13
2025-11-14查看详情 > -
Document: Meeting summary - PCWP/HCPWP and all eligible organisations meeting 18 November 2025-2025/12/9
2025-12-10查看详情 > -
Document: Consolidated 3-year rolling work plan for the Non-clinical domain 2026-2028-2026/1/21
2026-01-22查看详情 > -
Document: Electronic reporting to EudraVigilance - List of reference documents-2026/2/24
2026-02-27查看详情 >
