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Document: Minutes of the COMP meeting 4-6 November 2025-2026/1/15
2026-01-16查看详情 > -
Document: Minutes of the CHMP meeting 21-24 July 2025-2026/2/16
2026-02-26查看详情 > -
Document: List of medicinal products under additional monitoring-2026/3/25
2026-03-26查看详情 > -
Document: European Shortages Monitoring Platform (ESMP) User guide for national competent authorities-2026/4/29
2026-04-30查看详情 > -
User Fees and Refunds for Premarket Approval Applications and Device Biologics License Applications (Final)-2022/10/5
2022-11-15查看详情 > -
呼吸道合胞病毒感染药物临床试验技术指导原则-2023/4/12
2023-04-13查看详情 > -
国家药监局 海关总署关于泰吉利定等海关商品编号的公告（2023年第128号 ）-2023/10/13
2023-10-13查看详情 > -
Document: QRD veterinary product-information template version 9.1-2025/1/7
2025-01-08查看详情 > -
国家药监局综合司关于同意湖南省药品检验检测研究院增加生物制品批签发证明文件授权签字人的复函-2025/2/17
2025-02-18查看详情 > -
Document: European Medicines Agency pre-authorisation procedural advice for users of the centralised procedure: document with tracked changes-2025/3/25
2025-03-26查看详情 >
