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国家药监局药审中心关于发布《化学药品变更受理审查指南（试行）》的通告（2026年第34号）-2026/5/15
2026-05-17查看详情 > -
Document: CAT quarterly highlights and approved ATMPs - June 2026-2026/6/29
2026-06-30查看详情 > -
Regulatory and procedural guideline: List of centrally authorised products requiring a notification of a change for update of annexes-2022/11/18
2022-11-30查看详情 > -
Regulatory and procedural guideline: European Medicines Agency procedural advice on recommendations on unforeseen variations according to Article 5 of Commission Regulation (EC) No 1234/2008-2023/5/31
2023-06-01查看详情 > -
国家药监局药审中心关于发布《新药临床安全性评价技术指导原则》的通告（2023年第59号）-2023/12/1
2023-12-04查看详情 > -
Document: Agenda - Medicine Shortages (SPOC) Working Party 21 January 2025-2025/1/21
2025-01-22查看详情 > -
Page: Pre-authorisation guidance-2025/2/24
2025-02-25查看详情 > -
Document: Procedural guidance to scientific committeesꞌ members and experts on completing the European Medicines Agencyꞌs declaration of interests in the Experts Management Tool-2025/4/1
2025-04-02查看详情 > -
关于电子申报资料网络传输系统升级维护的通知-2025/5/9
2025-05-12查看详情 > -
Document: Superseded list of references supporting the assessment of Zingiber officinale Roscoe, rhizoma-2025/6/19
2025-06-20查看详情 >
