| Eurlex法規(guī)編號(hào)： |
2025/2086 |
| OJ編號(hào)： |
OJ L 2025/2086, 20.10.2025 |
| 中文標(biāo)題： |
2025年10月17日委員會(huì)實(shí)施條例(EU) 2025/2086：根據(jù)條例(EU) 2021/2282，關(guān)于健康技術(shù)評(píng)估，制定在歐盟層面對(duì)醫(yī)療器械和體外診斷醫(yī)療器械聯(lián)合臨床評(píng)估的準(zhǔn)備和更新過(guò)程中進(jìn)行互動(dòng)、信息交換及參與的程序規(guī)則，以及這些聯(lián)合臨床評(píng)估的模板 |
| 原文標(biāo)題： |
Commission Implementing Regulation (EU) 2025/2086 of 17 October 2025 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 medical devices and in vitro diagnostic medical devices at Union level, as well as templates for those joint clinical assessments |
| 發(fā)布日期 |
2025-10-20 |
| 原文鏈接 |
查看歐盟官網(wǎng)文件 |
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