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ICH guideline E19 on a selective approach to safety data collection in specific late-stage pre-approval or post-approval clinical trials - Scientific guideline (updated)-2023/10/6
2023-10-07查看详情 > -
Document: European Medicines Agency budget for 2025-2025/1/7
2025-01-08查看详情 > -
Document: Implementation strategy of ICH Guideline M12 on drug interaction studies-2025/2/13
2025-02-14查看详情 > -
Document: Annex to 24-27 March 2025 CHMP Agenda-2025/3/24
2025-03-25查看详情 > -
工业和信息化部等七部门关于印发《医药工业数智化转型实施方案（2025—2030年）》的通知-2025/4/24
2025-04-27查看详情 > -
国家药监局 财政部 市场监管总局 关于对药品医疗器械质量安全内部举报人举报实施奖励的公告（2025年第41号）-2025/6/5
2025-06-06查看详情 > -
Page: Fees payable to the European Medicines Agency: Fees, charges and remuneration for assessment procedures and services relating to medicinal products for human use-2025/7/10
2025-07-11查看详情 > -
Document: European Medicines Agency’s data protection notice for the use of EMA Authentication Services and Microsoft Entra ID-2025/8/19
2025-08-20查看详情 > -
Document: HMA-EMA joint Network Data Steering Group meeting - 17 July 2025-2025/9/29
2025-09-30查看详情 > -
Document: From laboratory to patients: How the safety of medicines is ensured in the Europen Union-2025/11/6
2025-11-07查看详情 >
