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Document: Timetable: Marketing authorisation renewal application-2025/7/17
2025-07-18查看详情 > -
国家药监局关于发布YY/T 0661—2017《外科植入物 半结晶型聚丙交酯聚合物和共聚物树脂》等3项医疗器械行业标准修改单的公告（2025年第81号）-2025/9/1
2025-09-02查看详情 > -
Document: SMS guidance for external users-2025/10/3
2025-10-08查看详情 > -
Document: List of eligible industry stakeholder organisations-2025/11/12
2025-11-13查看详情 > -
Page: Combination Products Operational Group-2025/12/9
2025-12-10查看详情 > -
Document: Questions and answers about the clinical study data proof-of-concept pilot for industry-2026/1/21
2026-01-22查看详情 > -
Page: EudraVigilance training and support-2026/2/24
2026-02-27查看详情 > -
Document: European Medicines Agency post-authorisation procedural advice for users of the centralised procedure-2026/3/27
2026-03-30查看详情 > -
Document: European Medicines Agency's data protection notice for Modelling and Simulation Pilot - Use of clinical study data for scientific advice-2026/5/7
2026-05-08查看详情 > -
Page: Website outages and upgrades-2026/6/22
2026-06-23查看详情 >
