Suppr超能文献

EQIPD 质量体系简介。

Introduction to the EQIPD quality system.

机构信息

PAASP, Heidelberg, Germany.

Department of Experimental Neurology, Charité Universitätsmedizin, Berlin, Germany.

出版信息

Elife. 2021 May 24;10:e63294. doi: 10.7554/eLife.63294.

Abstract

While high risk of failure is an inherent part of developing innovative therapies, it can be reduced by adherence to evidence-based rigorous research practices. Supported through the European Union's Innovative Medicines Initiative, the EQIPD consortium has developed a novel preclinical research quality system that can be applied in both public and private sectors and is free for anyone to use. The EQIPD Quality System was designed to be suited to boost innovation by ensuring the generation of robust and reliable preclinical data while being lean, effective and not becoming a burden that could negatively impact the freedom to explore scientific questions. EQIPD defines research quality as the extent to which research data are fit for their intended use. Fitness, in this context, is defined by the stakeholders, who are the scientists directly involved in the research, but also their funders, sponsors, publishers, research tool manufacturers, and collaboration partners such as peers in a multi-site research project. The essence of the EQIPD Quality System is the set of 18 core requirements that can be addressed flexibly, according to user-specific needs and following a user-defined trajectory. The EQIPD Quality System proposes guidance on expectations for quality-related measures, defines criteria for adequate processes (i.e. performance standards) and provides examples of how such measures can be developed and implemented. However, it does not prescribe any pre-determined solutions. EQIPD has also developed tools (for optional use) to support users in implementing the system and assessment services for those research units that successfully implement the quality system and seek formal accreditation. Building upon the feedback from users and continuous improvement, a sustainable EQIPD Quality System will ultimately serve the entire community of scientists conducting non-regulated preclinical research, by helping them generate reliable data that are fit for their intended use.

摘要

虽然开发创新疗法的固有风险很高,但通过坚持基于证据的严格研究实践,可以降低失败的风险。在欧盟创新药物倡议的支持下,EQIPD 联盟开发了一种新颖的临床前研究质量体系,该体系既可以应用于公共部门,也可以应用于私营部门,并且任何人都可以免费使用。EQIPD 质量体系旨在通过确保生成稳健可靠的临床前数据,同时保持精简、高效,并且不会成为阻碍探索科学问题的自由的负担,从而促进创新。EQIPD 将研究质量定义为研究数据适用于其预期用途的程度。在这种情况下,适应性由利益相关者定义,利益相关者是直接参与研究的科学家,但也包括他们的资助者、赞助商、出版商、研究工具制造商以及多站点研究项目中的同行等合作伙伴。EQIPD 质量体系的核心是 18 项核心要求,可以根据用户的特定需求和定义的轨迹灵活解决。EQIPD 质量体系提出了与质量相关措施的期望指南,定义了充足流程的标准(即绩效标准),并提供了如何制定和实施此类措施的示例。但是,它并没有规定任何预定的解决方案。EQIPD 还开发了工具(供可选使用),以支持用户实施该系统,并为成功实施质量系统并寻求正式认证的研究单位提供评估服务。在用户反馈和持续改进的基础上,一个可持续的 EQIPD 质量体系最终将为开展非监管临床前研究的整个科学家社区服务,帮助他们生成适用于其预期用途的可靠数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b225/8184207/0bbe6cddaf44/elife-63294-fig1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验