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Regulatory and procedural guideline: Table of decisions of labelling exemption requests falling under article 63 of Directive 2001/83/EC examined by the Quality Review of Documents (QRD) Group-2023/4/19
2023-04-24查看详情 > -
国家药监局综合司公开征求《药品监督管理行政处罚裁量适用规则（征求意见稿）》意见-2023/10/19
2023-11-06查看详情 > -
Document: Table of decisions of labelling exemption requests falling under article 63 of Directive 2001/83/EC examined by the Quality Review of Documents (QRD) Group-2025/1/9
2025-01-10查看详情 > -
Page: Interested Parties to the HMPC-2025/2/17
2025-02-18查看详情 > -
Document: CTIS newsflash - 25 March 2025-2025/3/25
2025-03-26查看详情 > -
国家药监局关于注销电子胃镜等10个医疗器械注册证书的公告（2025年第42号）-2025/4/30
2025-05-06查看详情 > -
Document: Agenda of the CVMP meeting 10-12 June 2025-2025/6/10
2025-06-11查看详情 > -
Document: European Medicines Agency pre-authorisation procedural advice for users of the centralised procedure-2025/7/15
2025-07-16查看详情 > -
国家药监局关于28批次不符合规定药品的通告（2025年第30号）-2025/8/27
2025-08-28查看详情 > -
Document: Minutes - Enpr-EMA Coordinating Group & networks meeting - June 2025-2025/10/2
2025-10-08查看详情 >
