Automating User Approval and Onboarding in Trusted Research Environments.

IF 2.2 Q3 HEALTH CARE SCIENCES & SERVICES
International Journal of Population Data Science Pub Date : 2026-07-06 eCollection Date: 2026-01-01 DOI:10.23889/ijpds.v11i5.3518
Justin Biddle, Simon Elwood-Thompson
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引用次数: 0

Abstract

At SeRP, we provide a suite of software and hardware that enables Trusted Research Environments (TREs) to securely manage access to their data. A critical aspect of this is user approval and onboarding. When a new user requests access to a TRE, the environment typically requires a series of checks-such as completion of researcher training, signing of data access agreements, and director approval. Individual projects may also have additional, project-specific requirements. Traditionally, this process is manual, involving document requests, recording checks, and periodic verification of continuing approvals. To address this, we have developed a modular solution that leverages Camunda for customizable workflows and DocuSeal for document and signature management. Camunda workflows not only request documents and approvals, but also verify whether users meet general and project-specific access criteria, allowing permissions to be adjusted automatically. The system performs regular checks to ensure user and membership validity, and custom workflows can be configured for each TRE or project. This approach significantly automates the onboarding process, reduces administrative overhead, and strengthens security while maintaining flexibility for diverse TRE requirements.

在可信的研究环境中自动化用户审批和登录。
在SeRP,我们提供了一套软件和硬件,使可信研究环境(TREs)能够安全地管理对其数据的访问。其中一个关键的方面是用户批准和登录。当新用户请求访问数据仓库时,环境通常需要进行一系列检查,例如完成研究人员培训、签署数据访问协议和主管批准。个别项目也可能有附加的、特定于项目的需求。传统上,这个过程是手动的,涉及文档请求、记录检查和持续批准的定期验证。为了解决这个问题,我们开发了一个模块化的解决方案,利用Camunda来定制工作流,利用DocuSeal来管理文档和签名。Camunda工作流不仅请求文件和批准,还验证用户是否符合一般和特定项目的访问标准,允许自动调整权限。系统执行定期检查,以确保用户和成员资格的有效性,并且可以为每个TRE或项目配置自定义工作流。这种方法显著地自动化了入职过程,减少了管理开销,并增强了安全性,同时保持了对不同TRE需求的灵活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.50
自引率
0.00%
发文量
386
审稿时长
20 weeks
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