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Document: Policy 44: European Medicines Agency policy on the handling of competing interests of scientific committees’ members and experts-2025/5/1
2025-05-06查看详情 > -
Page: Medicines for human use under evaluation-2025/6/12
2025-06-13查看详情 > -
国家药监局综合司关于公开征求《关于医疗器械分类调整有关工作的公告（征求意见稿）》意见的函-2025/7/17
2025-07-18查看详情 > -
国家药监局关于废止《医疗器械行业标准的制定 第1部分：阶段划分、代码和程序》等5项医疗器械行业标准的公告（2025年第80号）-2025/9/1
2025-09-02查看详情 > -
Document: Timetable: Companion diagnostic initial consultation - ATMP-2025/10/3
2025-10-08查看详情 > -
Document: Highlights – Fourth EMA-Vaccines Europe bilateral meeting-2025/11/12
2025-11-13查看详情 > -
Document: Combination Products Operational Group (COMBO) - Terms of reference-2025/12/9
2025-12-10查看详情 > -
国家药监局药审中心关于发布《药物临床试验中应用贝叶斯外部信息借用方法的指导原则（试行）》的通告（2026年第6号）-2026/1/21
2026-01-22查看详情 > -
Document: EudraVigilance support guide-2026/2/24
2026-02-27查看详情 > -
Document: European Medicines Agency pre-authorisation procedural advice for users of the centralised procedure-2026/3/27
2026-03-30查看详情 >
