首页 >
法规速递
-
Document: Agenda of the CVMP meeting 11-13 February 2025-2025/2/11
2025-02-12查看详情 > -
国家药监局关于废止《医用中心吸引系统通用技术条件》等2项医疗器械行业标准的公告（2025年第31号）-2025/3/19
2025-03-20查看详情 > -
Document: Business process description for orphan status management-2025/4/22
2025-04-23查看详情 > -
Document: Agenda - Workshop on the use of Bayesian statistics in clinical development-2025/6/3
2025-06-04查看详情 > -
Document: Minutes - PDCO minutes of the 20-23 May 2025 meeting-2025/7/8
2025-07-09查看详情 > -
Page: Good agricultural and collection practice for starting materials of herbal origin - Scientific guideline-2025/8/12
2025-08-13查看详情 > -
国家药监局关于发布YY/T 1996—2025《采用脑机接口技术的医疗器械 具备闭环功能的植入式 神经刺激器 感知与响应性能测试方法》医疗器械行业标准的公告（2025年第94号）-2025/9/28
2025-09-28查看详情 > -
Document: Member states contact points for translations review-2025/11/4
2025-11-05查看详情 > -
Document: Abbreviations used in EMA scientific committees and Coordination Group for Mutual Recognition and Decentralised Procedures (CMD) documents, and in relation to EMA’s regulatory activities-2025/12/3
2025-12-04查看详情 > -
General Wellness: Policy for Low Risk Devices-2026/1/6
2026-01-08查看详情 >
