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药你知道 | 《国家药监局关于发布优化全生命周期监管支持高端医疗器械创新发展有关举措的公告》系列解读（七）-2025/9/19
2025-09-22查看详情 > -
2025年10月27日中药品种保护受理公示-2025/10/27
2025-10-28查看详情 > -
Page: Grouping of variations: questions and answers-2025/11/26
2025-11-27查看详情 > -
Page: Plasma master file certificates-2025/12/19
2025-12-22查看详情 > -
Document: Start of procedure: Extension of marketing authorisation (12 December 2025 - 29 January 2026)-2026/2/4
2026-02-05查看详情 > -
Document: Minutes - HMA-EMA joint Network Data Steering Group meeting - 11 February 2026-2026/3/13
2026-03-16查看详情 > -
Document: PDCO minutes of the 24-27 February 2026 meeting-2026/4/13
2026-04-14查看详情 > -
Regulatory and procedural guideline: Products Management Services (PMS) - Implementation of International Organization for Standardization (ISO) standards for the identification of medicinal products (IDMP) in Europe - Chapter 7 (updated)-2023/01/18
2023-01-18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(update)-2023/7/31
2023-08-02查看详情 > -
2023年度药品审评报告-2024/2/4
2024-03-12查看详情 >
