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中药保护品种公告（第32号）（2025年 第116号）-2025/12/12
2025-12-15查看详情 > -
Document: European Medicines Agency’s data protection notice for EudraVigilance Human (EV)-2026/1/23
2026-01-26查看详情 > -
Document: Annual report on the use of the special contribution for orphan medicinal products - 2025-2026/3/3
2026-03-04查看详情 > -
Page: Opinions and letters of support on the qualification of novel methodologies for medicine development-2026/3/3/1
2026-04-01查看详情 > -
Document: Timetable: Initial (full) marketing authorisation application accelerated assessment timetables-2026/5/13
2026-05-14查看详情 > -
Regulatory and procedural guideline: European Medicines Agency post-authorisation procedural advice for users of the centralised procedure: document with track changes-2022/11/4
2022-11-30查看详情 > -
关于公开征求ICH《E6（R3）：药物临床试验质量管理规范（GCP）》指导原则及附件1草案的通知-2023/5/29
2023-05-30查看详情 > -
国家药监局药审中心关于发布《药品说明书（简化版）及药品说明书（大字版）编写指南》和《电子药品说明书（完整版）格式要求》的通告（2023年第56号）-2023/11/24
2023-11-28查看详情 > -
Document: New fee regulation Annex IV: General questions and answers-2025/1/20
2025-01-21查看详情 > -
Document: Infectious Diseases Working Party (IDWP) consolidated 3-year rolling work plan 2025-2027-2025/2/21
2025-02-24查看详情 >
