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Regulatory and procedural guideline: Guidance on parallel EMA / EUnetHTA 21 Joint Scientific Consultation-2022/10/6
2022-11-15查看详情 > -
国家药监局关于修订白芍总苷胶囊说明书的公告（2023年第48号）-2023/4/24
2023-04-25查看详情 > -
国家药监局关于发布仿制药参比制剂目录（第七十三批）的通告（2023年第54号）-2023/10/26
2023-11-06查看详情 > -
国家药监局关于修订人血白蛋白注射剂说明书的公告（2025年第5号）-2025/1/13
2025-01-14查看详情 > -
Document: Agenda of the COMP meeting 18-19 February 2025-2025/2/17
2025-02-18查看详情 > -
Document: List of medicinal products under additional monitoring-2025/3/26
2025-03-27查看详情 > -
Page: Website outages and upgrades-2025/4/30
2025-05-06查看详情 > -
Document: European Shortages Monitoring Platform (ESMP): Implementation guide for national competent authorities-2025/6/10
2025-06-11查看详情 > -
Page: Pre-authorisation guidance-2025/7/15
2025-07-16查看详情 > -
关于公开征求《预防用生物制品批准后药学变更管理方案技术指导原则（征求意见稿）》意见的通知-2025/8/28
2025-08-29查看详情 >
