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Document: CVMP work plan 2026-2025/12/12
2025-12-15查看详情 > -
Page: Environmental management-2026/1/26
2026-01-27查看详情 > -
Document: Darwin EU: Making health data count-2026/3/4
2026-03-05查看详情 > -
Document: Orphan medical devices regular process: 2026 timetable-2026/4/1
2026-04-02查看详情 > -
国家药监局综合司公开征求《关于化学原料药再注册管理等有关事项的公告（征求意见稿）》意见-2022/11/4
2022-11-30查看详情 > -
国家药监局药审中心关于发布《非阿片类术后镇痛新药临床试验设计技术指导原则》的通告（2023年第35号）-2023/6/9
2023-06-12查看详情 > -
关于公开征求《脑膜炎球菌疫苗临床试验技术指导原则（征求意见稿）》意见的通知-2023/12/7
2023-12-21查看详情 > -
Document: Guideline on specific adverse reaction follow-up questionnaires (Specific AR FUQ)-2025/1/22
2025-01-23查看详情 > -
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 >
