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Document: Records of data processing activity for women leadership development and mentoring activities-2026/3/17
2026-03-18查看详情 > -
国家药监局综合司公开征求《药品经营质量管理规范附录：药品零售连锁质量管理（征求意见稿）》意见-2026/4/20
2026-04-21查看详情 > -
Regulatory and procedural guideline: Validation checklist for Type II quality variations (updated)-2023/02/10
2023-02-10查看详情 > -
关于公开征求《化学仿制药参比制剂目录（第七十三批）》（征求意见稿）意见的通知-2023/8/30
2023-09-01查看详情 > -
国家药监局药审中心关于发布《化学药品注册受理审查指南（试行）》的通告（2025年第14号）-2025/2/9
2025-02-10查看详情 > -
Document: Drug-Eluting stent (DES) - Notified Body 2265 - 10/01/2025 - Expert decision and opinion in the context of the clinical evaluation consultation procedure (CECP)-2025/3/13
2025-03-14查看详情 > -
Document: Policy 26: Records management and archives policy-2025/4/15
2025-04-16查看详情 > -
Page: Quality of medicines questions and answers: Part 2-2025/5/28
2025-05-29查看详情 > -
Page: QRD guidance on the use of adopted abbreviations and pictograms on the packaging of veterinary medicinal products authorised via the centralised (CP), mutual recognition (MRP), decentralised (DCP), subsequent recognition (SRP) and national procedure
2025-07-02查看详情 > -
国家药监局药审中心关于发布《药审中心外聘专家增补名单（2025年第一批、第二批）》的通告（2025年第35号）-2025/8/6
2025-08-06查看详情 >
