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Document: Timetable: Post-authorisation measures (PAMs) assessed by PRAC - ATMP-2025/11/4
2025-11-05查看详情 > -
Page: Veterinary good pharmacovigilance practices (VGVP)-2025/12/4
2025-12-05查看详情 > -
Use of Bayesian Methodology in Clinical Trials of Drug and Biological Products-2026/1/9
2026-01-13查看详情 > -
Document: Concept paper on the need of a guideline on clinical investigation of medicinal products in the treatment of Myasthenia Gravis-2026/2/13
2026-02-14查看详情 > -
Document: Records of data processing activity for the handling of data subjects’ requests-2026/3/24
2026-03-25查看详情 > -
Document: European Medicines Agency’s Data Protection Notice for the use of Microsoft Applications: OneDrive, Outlook 365, Teams and SharePoint-2026/4/28
2026-04-29查看详情 > -
关于公开征求《新药临床安全性评价技术指导原则》意见的通知-2022/10/25
2022-11-14查看详情 > -
关于电子证照附件格式变更的通知-2023/03/29
2023-03-29查看详情 > -
关于公开征求《低分子量肝素类仿制药药学研究与评价技术指导原则(征求意见稿)》意见的通知-2023/9/28
2023-10-07查看详情 > -
Document: Rafoxanide (bovine and ovine milk): European Public MRL Assessment Report (EPMAR) - CVMP-2025/1/7
2025-01-08查看详情 >