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A workflow-driven approach to integrate generic software modules in a Trusted Third Party

机译:一种工作流程驱动的方法,可将通用软件模块集成到受信任的第三方中

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Background Cohort studies and registries rely on massive amounts of personal medical data. Therefore, data protection and information security as well as ethical aspects gain in importance and need to be considered as early as possible during the establishment of a study. Resulting legal and ethical obligations require a precise implementation of appropriate technical and organisational measures for a Trusted Third Party. Methods This paper defines and organises a consistent workflow-management to realize a Trusted Third Party. In particular, it focusses the technical implementation of a Trusted Third Party Dispatcher to provide basic functionalities (including identity management, pseudonym administration and informed consent management) and measures required to meet study specific conditions of cohort studies and registries. Thereby several independent open source software modules developed and provided by the MOSAIC project are used. This technical concept offers the necessary flexibility and extensibility to address legal and ethical requirements of individual scenarios. Results The developed concept for a Trusted Third Party Dispatcher allows mapping single process steps as well as individual requirements and characteristics of particular studies to workflows, which in turn can be combined to model complex Trusted Third Party processes. The uniformity of this approach permits unrestricted re-combination of the available functionalities (depending on the applied software modules) for various research projects. Conclusion The proposed approach for the technical implementation of an independent Trusted Third Party reduces the effort for scenario specific implementations as well as for maintenance. The applicability and the efficacy of the concept for a workflow-driven Trusted Third Party could be confirmed during the establishment of several nationwide studies (e.g. German Centre for Cardiovascular Research and the National Cohort).
机译:背景队列研究和注册中心依赖大量的个人医疗数据。因此,数据保护和信息安全以及道德方面变得越来越重要,需要在研究建立过程中尽早考虑。由此产生的法律和道德义务要求为受信任的第三方准确执行适当的技术和组织措施。方法本文定义并组织了一致的工作流管理以实现受信任的第三方。特别是,它着重于受信任的第三方调度程序的技术实施,以提供基本功能(包括身份管理,化名管理和知情同意管理)以及满足队列研究和注册表的研究特定条件所需的措施。因此,使用了由MOSAIC项目开发和提供的几个独立的开源软件模块。该技术概念提供了必要的灵活性和可扩展性,可以满足各个方案的法律和道德要求。结果可信第三方分派器的已开发概念允许将单个过程步骤以及个别研究的特定要求和特征映射到工作流,然后可以将其组合以对复杂的可信第三方过程建模。这种方法的统一性允许无限制地重新组合各种研究项目的可用功能(取决于所应用的软件模块)。结论提出的用于独立受信任第三方的技术实施的方法减少了针对特定情况的实施以及维护的工作量。在一些全国性研究(例如德国心血管研究中心和国家队列)的建立过程中,可以证实该概念对于工作流驱动的受信任第三方的适用性和有效性。

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