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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 > -
Page: Type-II variations: questions and answers-2026/3/27
2026-03-30查看详情 > -
Document: List of industry subject matter experts and list of planned calls for industry subject matter experts-2026/5/7
2026-05-08查看详情 > -
Scientific guideline: ICH M11 template - Step 2b-2022/10/26
2022-11-15查看详情 > -
Regulatory and procedural guideline: European Medicines Agency post-authorisation procedural advice for users of the centralised procedure-2023/4/25
2023-04-26查看详情 >
