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Eurlex法規(guī)編號：	(EU) 2024/2699
OJ編號：	OJ L, 2024/2699, 21.10.2024
中文標題：	2024年10月18日委員會實施條例(EU) 2024/2699：根據歐洲議會和理事會條例(EU) 2021/2282,，規(guī)定了成員國衛(wèi)生技術評估協(xié)調小組和委員會與歐洲藥品管理局合作的詳細程序規(guī)則,，其形式為就醫(yī)藥產品、醫(yī)療器械和體外診斷醫(yī)療器械的聯(lián)合臨床評估以及醫(yī)藥產品和醫(yī)療器械的聯(lián)合科學咨詢進行信息交流
原文標題：	Commission Implementing Regulation (EU) 2024/2699 of 18 October 2024 laying down, pursuant to Regulation (EU) 2021/2282 of the European Parliament and of the Council, detailed procedural rules for the cooperation of the Member State Coordination Group on Health Technology Assessment and the Commission with the European Medicines Agency in the form of exchange of information as regards the joint clinical assessment of medicinal products and medical devices and in vitro diagnostic medical devices and as regards the joint scientific consultation on medicinal products and medical devices
發(fā)布日期	2024-10-21
原文鏈接	查看歐盟官網文件