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国家药监局药审中心关于发布《化学药品仿制药上市许可申请模块二药学资料撰写要求（试行）》的通告（2025年第32号）-2025/8/28
2025-08-29查看详情 > -
Document: Agenda - Management Board meeting: 2 October 2025-2025/10/2
2025-10-08查看详情 > -
Document: Article 57 product data-2025/11/11
2025-11-12查看详情 > -
Document: New Approach Methodologies EU-IN Horizon Scanning Report-2025/12/9
2025-12-10查看详情 > -
Document: Annual report of the Good Clinical Practice Inspectors Working Group 2024-2026/1/20
2026-01-21查看详情 > -
Document: Record of data processing activity relating to Security Access Control System-2026/2/24
2026-02-27查看详情 > -
Page: Vaccine-preventable diseases: key facts-2026/3/26
2026-03-27查看详情 > -
国家药监局关于二丁胶囊和眠安宁颗粒转换为非处方药的公告（2026年第43号）-2026/5/6
2026-05-07查看详情 > -
Regulatory and procedural guideline: Data Quality Framework for EU medicines regulation-2022/10/10
2022-11-15查看详情 > -
国家药监局关于修订壮骨止痛胶囊和小儿咳喘灵制剂说明书的公告（2023年第45号）-2023/4/24
2023-04-25查看详情 >
