首页 >
法规速递
-
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 > -
Document: Agenda - Clinical trials information system information day webinar-2026/6/9
2026-06-10查看详情 > -
Document: Terms of reference for the cluster on pregnancy and lactation-2026/7/17
2026-07-19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 >
