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Document: Draft user manual for the eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) user interface (XEVMPDweb)-2025/12/10
2025-12-11查看详情 > -
Document: Scientific advice and protocol assistance adopted during the CHMP meeting 8-11 December 2025-2026/1/23
2026-01-26查看详情 > -
Page: Quality of medicines: questions and answers - Part 1-2026/3/2
2026-03-03查看详情 > -
Document: EU implementation strategy of ICH E2D(R1) Guideline - Post-approval safety data: Definitions and standards for management and reporting of individual case safety reports-2026/3/27
2026-03-30查看详情 > -
Document: Applications for new human medicines under evaluation: May 2026-2026/5/11
2026-05-12查看详情 > -
Page: Cookies-2026/6/24
2026-06-25查看详情 > -
Document: Sponsor guidance: New safety module on the annual safety report-2026/7/31
2026-08-02查看详情 > -
氯雷他定片生物等效性研究技术指导原则-2022/11/25
2022-11-25查看详情 > -
关于公开征求《化学仿制药参比制剂目录（第六十九批）》（征求意见稿）意见的通知-2023/5/4
2023-05-05查看详情 > -
Regulatory and procedural guideline: European Medicines Agency pre-authorisation procedural advice for users of the centralised procedure (updated)-2023/11/13
2023-11-15查看详情 >
