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关于公开征求《药品监管信息化标准体系（征求意见稿）》-2023/4/11
2023-04-14查看详情 > -
《药品经营和使用质量监督管理办法》政策解读-2023/10/13
2023-10-13查看详情 > -
Document: IRIS guide for applicants - How to create and submit scientific applications, for industry and individual applicants-2025/1/8
2025-01-09查看详情 > -
Page: Guideline on assessment and reporting of mechanistic models used in the context of model informed drug development-2025/2/14
2025-02-18查看详情 > -
Document: European Medicines Agency post-authorisation procedural advice for users of the centralised procedure: document with track changes-2025/3/25
2025-03-26查看详情 > -
Page: Vaccine-preventable diseases: key facts-2025/4/28
2025-04-29查看详情 > -
Document: QRD veterinary product-information template version 9.1-2025/6/5
2025-06-06查看详情 > -
国家药监局关于发布仿制药参比制剂目录（第九十四批）及调出参比制剂目录品种清单（第二批）的通告（2025年第26号）-2025/7/15
2025-07-16查看详情 > -
国家药监局综合司关于印发2025年化妆品标准立项计划的通知-2025/8/21
2025-08-22查看详情 > -
Document: Minutes of the CAT meeting 12-14 August 2025 - written procedure-2025/9/30
2025-10-08查看详情 >
