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Page: Interested Parties to the HMPC-2026/2/4
2026-02-05查看详情 > -
国家药监局关于批准注册235个医疗器械产品的公告（2026年2月）（2026年第25号）-2026/3/13
2026-03-16查看详情 > -
Page: CHMP opinions on consultation procedures on ancillary substances incorporated in a medical device-2026/4/10
2026-04-12查看详情 > -
Mpox: Development of Drugs and Biological Products; Guidance for Industry(Draft)-2023/01/19
2023-01-19查看详情 > -
Regulatory and procedural guideline: List of centrally authorised products requiring a notification of a change for update of annexes-2023/7/25
2023-07-28查看详情 > -
国家药监局关于修订滑膜炎制剂说明书的公告（2024年第20号）-2024/3/5
2024-03-12查看详情 > -
Page: Website outages and upgrades-2025/1/31
2025-02-05查看详情 > -
Document: Frequently asked questions on the European Shortages Monitoring Platform (ESMP)-2025/3/10
2025-03-11查看详情 > -
Document: Rules of procedure of the Emergency Task Force (ETF)-2025/4/11
2025-04-13查看详情 > -
Document: Timetable: Type II variation and worksharing application monthly assessment-2025/5/23
2025-05-26查看详情 >
