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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 > -
Document: Decision of the Executive Director on the access to financial and administrative incentives for micro, small and medium-sized enterprises-2026/3/25
2026-03-26查看详情 > -
Document: Minutes of the Management Board meeting: 12 March 2026-2026/5/4
2026-05-06查看详情 > -
境外生产药品上市后备案类变更问与答（一）-2026/6/16
2026-06-17查看详情 > -
In Vitro Permeation Test Studies for Topical Drug Products Submitted in ANDAs (Draft)-2022/10/21
2022-11-15查看详情 >
