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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 > -
Document: Explanatory note on the withdrawal of the interim guidance on enhanced safety surveillance for seasonal influenza vaccines in the EU-2025/12/4
2025-12-05查看详情 > -
国家药监局药审中心关于发布eCTD V3.2.2相关技术文件的通告（2026年第4号）-2026/1/15
2026-01-16查看详情 > -
国家药监局关于批准注册292个医疗器械产品的公告（2026年1月）（2026年第20号）-2026/2/25
2026-02-26查看详情 >
