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Document: Agenda - PDCO agenda of the 11-14 November 2025 meeting-2025/11/11
2025-11-12查看详情 > -
Page: Development and manufacture of synthetic peptides - Scientific guideline-2025/12/9
2025-12-10查看详情 > -
Document: Standard operating procedure for procedure to be followed when the incident management plan for medicines for veterinary use is triggered-2026/1/20
2026-01-21查看详情 > -
Page: ICH M4Q - The Common Technical Document for the registration of pharmaceuticals for human use - Quality - Scientific guideline-2026/2/20
2026-02-27查看详情 > -
Page: Clinical Trials Information System (CTIS): training and support-2026/3/26
2026-03-27查看详情 > -
Document: Minutes of the CAT meeting 18-20 March 2026-2026/5/5
2026-05-06查看详情 > -
Page: Languages on this website-2026/6/16
2026-06-17查看详情 > -
Document: European Medicines Agency’s data protection notice for meeting registration forms via EUSurvey-2026/7/24
2026-07-26查看详情 > -
Regulatory and procedural guideline: Guidance on parallel EMA / EUnetHTA 21 Joint Scientific Consultation-2022/10/6
2022-11-15查看详情 > -
国家药监局关于修订白芍总苷胶囊说明书的公告（2023年第48号）-2023/4/24
2023-04-25查看详情 >
