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国家药监局综合司关于同意吉林省药品检验研究院增加生物制品批签发证明文件授权签发人的复函-2023/9/27
2023-09-28查看详情 > -
Document: Annex to interim measures regarding notification of pharmacovigilance alerts by marketing authorisation holders under Regulation (EU) 2019/6: contact points-2025/1/6
2025-01-07查看详情 > -
Document: Consolidated 3-year work plan for the Emergency Task Force (ETF)-2025/2/11
2025-02-12查看详情 > -
国家药监局综合司关于印发2025年医疗器械行业标准制修订计划项目的通知-2025/3/19
2025-03-20查看详情 > -
Document: Business process description for pharmacovigilance-2025/4/22
2025-04-23查看详情 > -
Document: Product Management Service (PMS) – Frequently Asked Questions (FAQs)-2025/6/3
2025-06-04查看详情 > -
国家药监局关于注销咽鼓管压力测量仪等17个医疗器械注册证书的公告(2025年第66号)-2025/7/9
2025-07-10查看详情 > -
关于公开征求《罕见病用化学药物药学研究指导原则(征求意见稿)》意见的通知-2025/8/14
2025-08-15查看详情 > -
Document: List of medicines currently in PRIME scheme-2025/9/26
2025-09-28查看详情 > -
Document: QRD Form 2 and checklist for the submission of day +25 files - human-2025/11/4
2025-11-05查看详情 >