Multivariate statistical monitoring as applied to clean‐in‐place (CIP) and steam‐in‐place (SIP) operations in biopharmaceutical manufacturing |
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Authors: | Kevin Roy Cenk Undey Thomas Mistretta Gregory Naugle Manbir Sodhi |
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Affiliation: | 1. Amgen Inc., Operations Improvement, Industrial Engineering, W. Greenwich, RI;2. Amgen Inc., Operations Technology, Digital Development, Thousand Oaks, CA;3. Amgen Inc., Operations Technology, Process Development, W. Greenwich, RI;4. Dept. of Mechanical, University of Rhode Island, Systems and Industrial Engineering, Kingston, RI |
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Abstract: | Multivariate statistical process monitoring (MSPM) is becoming increasingly utilized to further enhance process monitoring in the biopharmaceutical industry. MSPM can play a critical role when there are many measurements and these measurements are highly correlated, as is typical for many biopharmaceutical operations. Specifically, for processes such as cleaning‐in‐place (CIP) and steaming‐in‐place (SIP, also known as sterilization‐in‐place), control systems typically oversee the execution of the cycles, and verification of the outcome is based on offline assays. These offline assays add to delays and corrective actions may require additional setup times. Moreover, this conventional approach does not take interactive effects of process variables into account and cycle optimization opportunities as well as salient trends in the process may be missed. Therefore, more proactive and holistic online continued verification approaches are desirable. This article demonstrates the application of real‐time MSPM to processes such as CIP and SIP with industrial examples. The proposed approach has significant potential for facilitating enhanced continuous verification, improved process understanding, abnormal situation detection, and predictive monitoring, as applied to CIP and SIP operations. © 2014 American Institute of Chemical Engineers Biotechnol. Prog., 30:505–515, 2014 |
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Keywords: | multivariate statistical process monitoring clean‐in‐place steam‐in‐place biopharmaceutical manufacturing continued verification |
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