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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 > -
Monoclonal Antibodies: Streamlined Nonclinical Safety Studies-2025/12/2
2025-12-04查看详情 > -
Page: Financial management and budgetary reporting-2026/1/8
2026-01-09查看详情 >
