首页 >
法规速递
-
Document: HMPC: overview of assessment work - priority list-2025/5/15
2025-05-16查看详情 > -
2025年6月25日中药品种保护受理公示-2025/6/25
2025-06-26查看详情 > -
Document: Template for scientific document for paediatric investigation plan or product-specific waiver-2025/7/28
2025-07-29查看详情 > -
关于公开征求《艾滋病免疫功能重建不全治疗药物临床试验技术指导原则（征求意见稿）》意见的通知-2025/9/12
2025-09-12查看详情 > -
Document: Process for the electronic submission of medicinal product information - Chapter 3-2025/10/16
2025-10-17查看详情 > -
国家药监局关于发布药品生产企业出口药品检查和出口证明管理规定的公告（2025年第113号）-2025/11/21
2025-11-24查看详情 > -
Enhancing Participation in Clinical Trials — Eligibility Criteria, Enrollment Practices, and Trial Designs-2025/12/15
2025-12-16查看详情 > -
Page: Questions and answers on how to use a CEP in the context of a Marketing Authorisation Application or a Marketing Authorisation Variation-2026/1/28
2026-01-29查看详情 > -
中药保护品种公告（第35号）（2026年第22号）-2026/3/9
2026-03-10查看详情 > -
Document: CHMP PROM minutes for the meeting on 12 May 2025-2026/4/7
2026-04-08查看详情 >
