Eurlex法規(guī)編號: |
(EU) 2024/1381 |
OJ編號: |
OJ L, 2024/1381, 24.5.2024 |
中文標(biāo)題: |
2024年5月23日委員會實(shí)施條例(EU) 2024/1381:根據(jù)條例(EU) 2021/2282,關(guān)于衛(wèi)生技術(shù)評估,制定了歐盟層面人類使用藥品聯(lián)合臨床評估的準(zhǔn)備和更新過程中的互動、信息交換和參與程序規(guī)則,以及這些聯(lián)合臨床評估模板 |
原文標(biāo)題: |
Commission Implementing Regulation (EU) 2024/1381 of 23 May 2024 laying down, pursuant to Regulation (EU) 2021/2282 on health technology assessment, procedural rules for the interaction during, exchange of information on, and participation in, the preparation and update of joint clinical assessments of medicinal products for human use at Union level, as well as templates for those joint clinical assessments |
發(fā)布日期 |
2024-05-24 |
原文鏈接 |
查看歐盟官網(wǎng)文件 |
閱讀:508次