首页 >
法规速递
-
国家药监局关于注销氯雷他定片等80个药品注册证书的公告（2025年第102号）-2025/10/15
2025-10-16查看详情 > -
Document: List of European Union reference dates (EURD) and frequency of submission of periodic safety update reports (PSURs)-2025/11/19
2025-11-20查看详情 > -
Page: Podcast: Inside EMA-2025/12/15
2025-12-16查看详情 > -
Document: List of medicinal products under additional monitoring-2026/1/28
2026-01-29查看详情 > -
Document: Highlight report - Combination Products Operational Group (COMBO) - In Vitro Diagnostics stream - February 2026-2026/3/6
2026-03-09查看详情 > -
Document: PRAC recommendations on signals adopted at the 9-12 March 2026 PRAC meeting-2026/4/7
2026-04-08查看详情 > -
ICH M12 on drug interaction studies - Scientific guideline-2022/12/12
2022-12-13查看详情 > -
国家药监局关于发布仿制药参比制剂目录（第六十九批）的通告（2023年第27号）-2023/6/26
2023-06-27查看详情 > -
关于公开征求《已上市境外生产药品转移至境内生产的药品上市注册申请申报资料要求（治疗用生物制品）（征求意见稿）》意见的通知-2023/12/22
2024-01-03查看详情 > -
国家药监局综合司关于印发2025年药品检验能力验证计划的通知 -2025/1/23
2025-01-23查看详情 >
