首页 >
法规速递
-
Document: Network Data Steering Group workplan 2025-2028-2025/5/13
2025-05-14查看详情 > -
关于公开征求ICH《E21：临床试验中纳入妊娠和哺乳期女性》指导原则草案意见的通知-2025/6/20
2025-06-23查看详情 > -
Document: Table of decisions of labelling exemption requests falling under article 63 of Directive 2001/83/EC examined by the Quality Review of Documents (QRD) Group-2025/7/25
2025-07-27查看详情 > -
Document: Regulatory Procedure Management (RPM) for the Product Lifecycle Management (PLM) - Frequently asked questions-2025/9/10
2025-09-11查看详情 > -
Document: Management Board - Outcome of written procedures finalised during the period from 29 June to 22 September 2025-2025/10/14
2025-10-15查看详情 > -
Page: Medicines for human use under evaluation-2025/11/18
2025-11-19查看详情 > -
Document: Minutes of the CVMP meeting 4-6 November 2025-2025/12/12
2025-12-15查看详情 > -
Page: Handling competing interests-2026/1/27
2026-01-28查看详情 > -
Page: Clinical trials in human medicines-2026/3/5
2026-03-06查看详情 > -
《国家药监局关于“人工智能+药品监管”的实施意见》政策解读-2026/4/2
2026-04-03查看详情 >
