Good Statistical Monitoring: A Flexible Open-Source Tool to Detect Risks in Clinical Trials.

IF 2 4区 医学 Q4 MEDICAL INFORMATICS Therapeutic innovation & regulatory science Pub Date : 2024-09-01 Epub Date: 2024-05-09 DOI:10.1007/s43441-024-00651-4
George Wu, Spencer Childress, Zhongkai Wang, Matt Roumaya, Colleen McLaughlin Stern, Chelsea Dickens, Jeremy Wildfire
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Abstract

Background: Risk-based quality management is a regulatory-recommended approach to manage risk in a clinical trial. A key element of this strategy is to conduct risk-based monitoring to detect potential risks to critical data and processes earlier. However, there are limited publicly available tools to perform the analytics required for this purpose. Good Statistical Monitoring is a new open-source solution developed to help address this need.

Methods: A team of statisticians, data scientists, clinicians, data managers, clinical operations, regulatory, and quality compliance staff collaborated to design Good Statistical Monitoring, an R package, to flexibly and efficiently implement end-to-end analyses of key risks. The package currently supports the mapping of clinical trial data from a variety of formats, evaluation of 12 key risk indicators, interactive visualization of analysis results, and creation of standardized reports.

Results: The Good Statistical Monitoring package is freely available on GitHub and empowers clinical study teams to proactively monitor key risks. It employs a modular workflow to perform risk assessments that can be customized by replacing any workflow component with a study-specific alternative. Results can be exported to other clinical systems or can be viewed as an interactive report to facilitate follow-up risk mitigation. Rigorous testing and qualification are performed as part of each release to ensure package quality.

Conclusions: Good Statistical Monitoring is an open-source solution designed to enable clinical study teams to implement statistical monitoring of critical risks, as part of a comprehensive risk-based quality management strategy.

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良好的统计监测:检测临床试验风险的灵活开源工具。
背景:基于风险的质量管理是监管机构推荐的一种管理临床试验风险的方法。该策略的一个关键要素是进行基于风险的监控,以尽早发现关键数据和流程的潜在风险。然而,目前可用于执行这一目的所需分析的公开工具非常有限。Good Statistical Monitoring 是一种新的开源解决方案,旨在帮助满足这一需求:一个由统计学家、数据科学家、临床医生、数据管理人员、临床运营、监管和质量合规人员组成的团队合作设计了一个 R 软件包 Good Statistical Monitoring,以灵活高效地实施关键风险的端到端分析。该软件包目前支持多种格式的临床试验数据映射、12 个关键风险指标的评估、分析结果的交互式可视化以及标准化报告的创建:Good Statistical Monitoring 软件包可在 GitHub 上免费下载,使临床研究团队能够主动监控关键风险。它采用模块化工作流程来执行风险评估,可以通过用特定研究的替代方案替换任何工作流程组件来进行定制。评估结果可导出到其他临床系统,也可作为交互式报告查看,以方便后续风险缓解工作。每次发布都会进行严格的测试和鉴定,以确保软件包的质量:作为基于风险的全面质量管理策略的一部分,Good Statistical Monitoring 是一个开源解决方案,旨在帮助临床研究团队实施关键风险的统计监测。
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来源期刊
Therapeutic innovation & regulatory science
Therapeutic innovation & regulatory science MEDICAL INFORMATICS-PHARMACOLOGY & PHARMACY
CiteScore
3.40
自引率
13.30%
发文量
127
期刊介绍: Therapeutic Innovation & Regulatory Science (TIRS) is the official scientific journal of DIA that strives to advance medical product discovery, development, regulation, and use through the publication of peer-reviewed original and review articles, commentaries, and letters to the editor across the spectrum of converting biomedical science into practical solutions to advance human health. The focus areas of the journal are as follows: Biostatistics Clinical Trials Product Development and Innovation Global Perspectives Policy Regulatory Science Product Safety Special Populations
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