首页 >
法规速递
-
Document: Regulatory Science - Research needs - 2025 update-2025/7/18
2025-07-21查看详情 > -
Document: Decision of the Executive Director on rules governing the secondment of national experts to the EMA (from 1 October 2025)-2025/9/2
2025-09-03查看详情 > -
Document: Questions & Answers on the impact of Mutual Recognition Agreement (MRA) between the European Union and the United States as of 1st October 2025-2025/10/7
2025-10-08查看详情 > -
Page: ICH E21 guideline on inclusion of pregnant and breastfeeding individuals in clinical trials – Scientific guideline-2025/11/13
2025-11-14查看详情 > -
Document: Article 57 product data-2025/12/10
2025-12-11查看详情 > -
Cuffless Non-invasive Blood Pressure Measuring Devices – Clinical Performance Testing and Evaluation-2026/1/23
2026-01-23查看详情 > -
Document: Info sheet - Orphan medicines in the EU-2026/2/27
2026-02-28查看详情 > -
Document: Outcome of the public consultation on the Data Quality Framework for EU Medicines Regulation: application to Real-World Data-2026/3/27
2026-03-30查看详情 > -
国家药监局关于44批次不符合规定化妆品的通告（2026年第16号）-2026/5/9
2026-05-11查看详情 > -
国家药监局药审中心关于发布 《组织患者参与药物研发的一般考虑指导原则（试行）》的通告（2022年第46号）-2022/11/25
2022-11-25查看详情 >
