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Page: Good distribution practice-2025/2/24
2025-02-25查看详情 > -
Document: Template - Request for advice on the orphan device status pursuant to Article 61(2) of Regulation (EU) 2017/745 and MDCG 2024-10-2025/4/1
2025-04-02查看详情 > -
Document: Minutes of the HMPC meeting 17-19 March 2025-2025/5/12
2025-05-13查看详情 > -
Document: Agenda - EMA’s 30th anniversary scientific conference-2025/6/19
2025-06-20查看详情 > -
Document: LifeGlobal Media - Procedural steps and scientific information after initial consultation (archive)-2025/7/24
2025-07-25查看详情 > -
Page: Union Product Database: release notes-2025/9/9
2025-09-10查看详情 > -
Document: Annex to agenda of the CHMP meeting 13-16 October 2025-2025/10/13
2025-10-14查看详情 > -
图解海报 | 《国家药监局关于深化化妆品监管改革促进产业高质量发展的意见》系列解读（一）-2025/11/18
2025-11-19查看详情 > -
Document: ICH E22 Guideline on general considerations for patient preference studies - Step 2b-2025/12/12
2025-12-15查看详情 > -
国家药监局关于适用《M14:使用真实世界证据进行药品安全性评估的非干预性研究：规划、设计、分析和报告的一般原则》国际人用药品 注册技术协调会指导原则的公告（2026年第16号）-2026/1/27
2026-01-28查看详情 >
