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Multivariate Monitoring Workflow for Formulation Fill and Finish Processes

机译:配方填充和完成过程的多变量监控工作流

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摘要

Process monitoring is a critical task in ensuring the consistent quality of the final drug product in biopharmaceutical formulation, fill, and finish (FFF) processes. Data generated during FFF monitoring includes multiple time series and high-dimensional data, which is typically investigated in a limited way and rarely examined with multivariate data analysis (MVDA) tools to optimally distinguish between normal and abnormal observations. Data alignment, data cleaning and correct feature extraction of time series of various FFF sources are resource-intensive tasks, but nonetheless they are crucial for further data analysis. Furthermore, most commercial statistical software programs offer only nonrobust MVDA, rendering the identification of multivariate outliers error-prone. To solve this issue, we aimed to develop a novel, automated, multivariate process monitoring workflow for FFF processes, which is able to robustly identify root causes in process-relevant FFF features. We demonstrate the successful implementation of algorithms capable of data alignment and cleaning of time-series data from various FFF data sources, followed by the interconnection of the time-series data with process-relevant phase settings, thus enabling the seamless extraction of process-relevant features. This workflow allows the introduction of efficient, high-dimensional monitoring in FFF for a daily work-routine as well as for continued process verification (CPV).
机译:在生物制药配方,填充和完成(FFF)过程中,过程监控是确保最终药品质量始终如一的关键任务。在FFF监视期间生成的数据包括多个时间序列和高维数据,通常以有限的方式进行调查,很少使用多变量数据分析(MVDA)工具进行检查以最佳地区分正常观察结果和异常观察结果。各种FFF源的数据对齐,数据清理和正确的时间序列特征提取是资源密集型任务,但是它们对于进一步的数据分析至关重要。此外,大多数商业统计软件程序仅提供非稳健的MVDA,从而使多变量离群值的识别容易出错。为了解决此问题,我们旨在为FFF流程开发一种新颖的,自动化的,多变量的流程监控工作流程,该流程能够可靠地识别与流程相关的FFF功能中的根本原因。我们演示了算法的成功实现,该算法能够对齐数据并清除来自各种FFF数据源的时间序列数据,然后将时间序列数据与过程相关的相位设置进行互连,从而实现与过程相关的无缝提取特征。该工作流程允许在FFF中引入高效的高维监视,以进行日常工作例程以及持续的过程验证(CPV)。

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