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Multivariate Monitoring Workflow for Formulation, Fill and Finish Processes
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 li...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7356889/ https://www.ncbi.nlm.nih.gov/pubmed/32503165 http://dx.doi.org/10.3390/bioengineering7020050 |
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author | Pretzner, Barbara Taylor, Christopher Dorozinski, Filip Dekner, Michael Liebminger, Andreas Herwig, Christoph |
author_facet | Pretzner, Barbara Taylor, Christopher Dorozinski, Filip Dekner, Michael Liebminger, Andreas Herwig, Christoph |
author_sort | Pretzner, Barbara |
collection | PubMed |
description | 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). |
format | Online Article Text |
id | pubmed-7356889 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-73568892020-07-22 Multivariate Monitoring Workflow for Formulation, Fill and Finish Processes Pretzner, Barbara Taylor, Christopher Dorozinski, Filip Dekner, Michael Liebminger, Andreas Herwig, Christoph Bioengineering (Basel) Article 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). MDPI 2020-06-03 /pmc/articles/PMC7356889/ /pubmed/32503165 http://dx.doi.org/10.3390/bioengineering7020050 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Pretzner, Barbara Taylor, Christopher Dorozinski, Filip Dekner, Michael Liebminger, Andreas Herwig, Christoph Multivariate Monitoring Workflow for Formulation, Fill and Finish Processes |
title | Multivariate Monitoring Workflow for Formulation, Fill and Finish Processes |
title_full | Multivariate Monitoring Workflow for Formulation, Fill and Finish Processes |
title_fullStr | Multivariate Monitoring Workflow for Formulation, Fill and Finish Processes |
title_full_unstemmed | Multivariate Monitoring Workflow for Formulation, Fill and Finish Processes |
title_short | Multivariate Monitoring Workflow for Formulation, Fill and Finish Processes |
title_sort | multivariate monitoring workflow for formulation, fill and finish processes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7356889/ https://www.ncbi.nlm.nih.gov/pubmed/32503165 http://dx.doi.org/10.3390/bioengineering7020050 |
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