首页 >
法规速递
-
国家药监局关于批准注册204个医疗器械产品的公告（2025年10月）（2025年第111号）-2025/11/11
2025-11-12查看详情 > -
Page: European Surveillance of Veterinary Antimicrobial Consumption (ESVAC): 2009 - 2023-2025/12/9
2025-12-10查看详情 > -
Document: Applications for new human medicines under evaluation: January 2026-2026/1/20
2026-01-21查看详情 > -
Document: Minutes of the CVMP meeting 13-15 January 2026-2026/2/20
2026-02-27查看详情 > -
Document: Clinical Trial Information System (CTIS) - Sponsor handbook-2026/3/26
2026-03-27查看详情 > -
Page: Quality of medicines: questions and answers - Part 2-2026/5/5
2026-05-06查看详情 > -
Scientific guideline: ICH guideline E19 on a selective approach to safety data collection in specific late-stage pre-approval or post-approval clinical trials - Step5-2022/10/6
2022-11-15查看详情 > -
Scientific guideline: Reflection paper on establishing efficacy based on single-arm trials submitted as pivotal evidence in a marketing authorisation-2023/4/21
2023-04-24查看详情 > -
国家药监局综合司公开征求《药品现代物流规范化建设的指导意见（征求意见稿）》意见-2023/10/24
2023-11-06查看详情 > -
国家药监局药审中心关于发布《预防用猴痘疫苗非临床有效性研究技术指导原则（试行）》的通告（2025年第4号）-2025/1/10
2025-01-13查看详情 >
