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Regulatory and procedural guideline: European Medicines Agency guidance for applicants seeking scientific advice and protocol assistance with track-changes-2022/10/14
2022-11-15查看详情 > -
国家药监局关于适用《E19：在特定的上市前后期或上市后临床试验中选择性收集安全性数据》国际人用药品注册技术协调会指导原则的公告（2023年第56号）-2023/4/24
2023-04-25查看详情 > -
关于公开征求《治疗慢性心力衰竭药物临床试验技术指导原则（征求意见稿）》意见的通知-2023/10/30
2023-11-06查看详情 > -
Document: Timetable: Initial (Full) marketing authorisation application - ATMP-2025/1/14
2025-01-15查看详情 > -
Document: Quick guide: How to search, view and download a Clinical Trial and a Clinical Trial Application (sponsors) - CTIS Training Programme - Module 09-2025/2/18
2025-02-19查看详情 > -
Document: Product Management Service (PMS) roadmap-2025/3/26
2025-03-27查看详情 > -
Document: List of European Union reference dates (EURD) and frequency of submission of periodic safety update reports (PSURs)-2025/4/30
2025-05-06查看详情 > -
图解海报 |《医疗器械网络销售质量管理规范》系列解读（一）-2025/6/11
2025-06-12查看详情 > -
Page: Scientific and technical recommendations: Veterinary Medicines Regulation-2025/7/16
2025-07-17查看详情 > -
Document: List of centrally authorised products with safety-related changes to the product information-2025/8/29
2025-09-01查看详情 >
