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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 > -
国家药监局关于发布医疗器械网络销售质量管理规范的公告（2025年第46号）-2025/4/28
2025-04-29查看详情 > -
M11 Technical Specification: Clinical Electronic Structured Harmonised Protocol-2025/6/6
2025-06-06查看详情 > -
Document: Antimicrobial Sales and Use (ASU) Platform: Release notes-2025/7/11
2025-07-14查看详情 > -
Document: PRAC recommendations on signals adopted at the 7-10 July 2025 PRAC meeting-2025/8/20
2025-08-21查看详情 >
