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Page: Qualification of novel methodologies for medicine development-2026/7/7
2026-07-08查看详情 > -
Document: Reliance for postauthorisation changes (PACs): Mid-pilot review-2026/8/13
2026-08-14查看详情 > -
同名同方药研究技术指导原则（试行）-2022/12/27
2022-12-29查看详情 > -
《药品标准管理办法》政策解读-2023/7/5
2023-07-07查看详情 > -
国家药监局综合司关于印发药品网络交易第三方平台检查指南（试行）的通知 药监综药管函〔2023〕691号-2024/1/5
2024-01-19查看详情 > -
Document: Exelon-H-C-PSUSA-00002654-202401 : EPAR - Scientific conclusions and grounds for the variation to the terms of the marketing authorisation-2025/1/28
2025-02-05查看详情 > -
Page: Procurement-2025/3/3
2025-03-04查看详情 > -
Document: Innovation Task Force (ITF) briefing meeting request form-2025/4/8
2025-04-09查看详情 > -
关于港澳已上市传统口服中成药内地上市注册沟通交流服务有关事宜的通知-2025/5/19
2025-05-20查看详情 > -
国家药监局综合司公开征求《医疗器械注册自检管理规定实施指南（征求意见稿）》意见-2025/6/26
2025-06-27查看详情 >
