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Document: Outcome of Public consultation on Policy 0044 - Summary of comments and EMA feedback-2025/1/14
2025-01-15查看详情 > -
Document: European Medicines Agency post-authorisation procedural advice for users of the centralised procedure-2025/2/18
2025-02-19查看详情 > -
Document: Annual report of the Good Manufacturing and Distribution Practice Inspectors Working Group 2024-2025/3/27
2025-03-28查看详情 > -
Document: Policy 58: European Medicines Agency policy on the handling of competing interests of Management Board members-2025/5/1
2025-05-06查看详情 > -
Document: Agenda - Workshop on the use of Bayesian statistics in clinical development-2025/6/12
2025-06-13查看详情 > -
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 >
