首页> 外文期刊>Journal of cystic fibrosis: official journal of the European Cystic Fibrosis Society >Guideline on the design and conduct of cystic fibrosis clinical trials: the European Cystic Fibrosis Society-Clinical Trials Network (ECFS-CTN).
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Guideline on the design and conduct of cystic fibrosis clinical trials: the European Cystic Fibrosis Society-Clinical Trials Network (ECFS-CTN).

机译:囊性纤维化临床试验的设计和实施指南:欧洲囊性纤维化学会临床试验网络(ECFS-CTN)。

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摘要

We describe the rationale for disease specific research networks in general as well as the aims and function of the European Cystic Fibrosis Society-Clinical Trials Network (ECFS-CTN) specifically. The ECFS-CTN was founded in 2009 with the aim of improving the quality and quantity of clinical research in the area of cystic fibrosis (CF) in Europe. A network of 18 clinical trial sites in 8 European countries was established according to uniform state-of-the-art quality criteria. To support the ECFS-CTN in the acquisition, planning and conduct of clinical trials, the network is equipped with a coordinating centre, steering and executive committees, and committees for protocol review, standardization, training and networking as well as a data safety monitoring board. A strong partnership with European CF patient parent organizations aims to increase awareness of the need for efficient clinical research and the participation of patients in clinical trials.
机译:我们总体上描述了针对特定疾病的研究网络的基本原理,以及欧洲囊性纤维化学会临床试验网络(ECFS-CTN)的目标和功能。 ECFS-CTN成立于2009年,旨在提高欧洲囊性纤维化(CF)领域临床研究的质量和数量。根据统一的最新质量标准,在8个欧洲国家/地区建立了由18个临床试验站点组成的网络。为了支持ECFS-CTN进行临床试验的获取,计划和进行,该网络配备了一个协调中心,指导委员会和执行委员会,以及用于协议审查,标准化,培训和联网的委员会,以及一个数据安全监控委员会。与欧洲CF患者家长组织的牢固合作关系旨在提高人们对有效临床研究的必要性以及患者参与临床试验的认识。

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