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Document: List of clinical evaluation consultation procedure (CECP) opinions issued for medical devices awaiting finalisation of conformity assessment-2026/2/3
2026-02-04查看详情 > -
Document: DARWIN EU Advisory Board: Membership-2026/3/11
2026-03-12查看详情 > -
Document: Clinical Trial Information System (CTIS) - Sponsor Frequently Asked Questions (FAQ)-2026/4/9
2026-04-10查看详情 > -
Regulatory and procedural guideline: European Medicines Agency pre-authorisation procedural advice for users of the centralised procedure (updated)-2022/12/21
2022-12-21查看详情 > -
国家药监局关于药物非临床研究质量管理规范认证公告(第6号) (2023年第94号)-2023/7/25
2023-07-28查看详情 > -
Draft Guidance: Use of Data Monitoring Committees in Clinical Trials-2024/2/12
2024-03-11查看详情 > -
Page: Union Product Database: release notes-2025/1/30
2025-02-05查看详情 > -
Document: European Shortages Monitoring Platform (ESMP) User guide for marketing authorisation holders-2025/3/10
2025-03-11查看详情 > -
Document: List of industry subject matter experts and list of planned calls for industry subject matter experts-2025/4/10
2025-04-11查看详情 > -
Document: Start of Union reviews adopted during the CHMP meeting of 19-22 May 2025-2025/5/23
2025-05-26查看详情 >
