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Page: Notifying a change of marketing status-2025/3/25
2025-03-26查看详情 > -
Document: CTIS newsflash - 29 April 2025-2025/4/29
2025-04-30查看详情 > -
关于公开征求《先进治疗药品的范围、归类和释义（征求意见稿）》意见的通知-2025/6/10
2025-06-11查看详情 > -
Document: Checklist for the submission of product information annexes and Annex A (if applicable) for minor procedures without linguistic review - human-2025/7/15
2025-07-16查看详情 > -
Page: Development of the Clinical Trials Information System-2025/8/26
2025-08-27查看详情 > -
Page: Accessibility-2025/10/1
2025-10-08查看详情 > -
Document: Pharmacovigilance-related regulatory recommendations for centrally authorised veterinary medicinal products during 2025-2025/11/10
2025-11-11查看详情 > -
Document: Programme - Joint HMA/EMA multi-stakeholder workshop on Patient Registries December 2025-2025/12/8
2025-12-09查看详情 > -
Page: Submission deadlines for orphan designations-2026/1/19
2026-01-20查看详情 > -
Document: Draft guideline on quality aspects of mRNA vaccines for veterinary use-2026/2/20
2026-02-27查看详情 >
