MIT CAACB Risk Assessment Case Study: Assessing Virus Cross-Contamination Risk between Two Simultaneous Processes in an Open Biomanufacturing Facility.

Q3 Medicine
Andrea L Koenigsberg, Veronica Fowler, Reuben Domike, Audrey Brussel, Paul W Barone, Flora J Keumurian, James Leung, Michael E Wiebe, Michael T Brewer, Shawn Chan, Nicolas Dumey, Anne Fournillier, Marcella Goodnight, Johanna Kindermann, Richard Leavy, Buyoung Lee, Stefan Minning, Marie Murphy, Eric Myers, Armen Nahabedian, Kavita Nanda, Sandi Parriott, G K Raju, Ciaran Scallan, Stephanie Schoch, Joe Shiminsky, Bonnie Shum, Sebastian Teitz, Bernice Westrek, Stacy Springs
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引用次数: 0

Abstract

Some members of MIT's Consortium on Adventitious Agent Contamination in Biomanufacturing (CAACB) previously published content on the "Quality Risk Management in the Context of Viral Contamination", which described tools, procedures, and methodologies for assessing and managing the risk of a potential virus contamination in cell culture processes. To address the growing industry interest in moving manufacturing toward open ballrooms with functionally closed systems and to demonstrate how the ideas of risk management can be leveraged to perform a risk assessment, CAACB conducted a case study exercise of these new manufacturing modalities. In the case study exercise, a cross-functional team composed of personnel from many of CAACB's industry membership collaboratively assessed the risks of viral cross-contamination between a human and non-human host cell system in an open manufacturing facility. This open manufacturing facility had no walls to provide architectural separation of two processes occurring simultaneously, specifically a recombinant protein perfusion cell culture process using the human cell line, HEK-293 (Process 1) and a downstream postviral filtration unit operation (Process 2) of a recombinant protein produced in CHO cells. This viral risk assessment focused on cross-contamination of the Process 2 filtration unit operation after the Process 1 perfusion bioreactor was contaminated with a virus that went undetected. The workflow for quality risk management that is recommended by the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) was followed, which included identifying and mapping the manufacturing process, defining the risk question, risk evaluation, and risk control. The case study includes a completed Failure Mode and Effects Analysis (FMEA) to provide descriptions of the specific risks and corresponding recommended risk reduction actions.

麻省理工学院CAACB风险评估案例研究:评估开放式生物制造设施中两个同步过程之间的病毒交叉污染风险。
麻省理工学院生物制造中不确定因子污染联盟(CAACB)的一些成员先前发表了关于“病毒污染背景下的质量风险管理”的内容,其中描述了评估和管理细胞培养过程中潜在病毒污染风险的工具、程序和方法。为了满足日益增长的行业对将制造业转向具有功能封闭系统的开放式舞厅的兴趣,并演示如何利用风险管理的思想来执行风险评估,CAACB对这些新的制造模式进行了案例研究。在案例研究练习中,一个由来自CAACB许多行业成员的人员组成的跨职能团队协同评估了开放式生产设施中人类和非人类宿主细胞系统之间病毒交叉污染的风险。这个开放式的生产设施没有墙来提供同时发生的两个过程的结构分离,特别是使用人类细胞系HEK-293的重组蛋白灌注细胞培养过程(过程1)和CHO细胞中产生的重组蛋白的下游病毒后过滤单元操作(过程2)。本次病毒风险评估的重点是在流程1灌注生物反应器被未检测到的病毒污染后,流程2过滤单元操作的交叉污染。遵循了国际人用药品技术要求协调委员会(ICH)推荐的质量风险管理工作流程,其中包括识别和绘制生产过程、定义风险问题、风险评估和风险控制。案例研究包括完整的失效模式和影响分析(FMEA),以提供具体风险的描述和相应的风险降低措施建议。
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
1.90
自引率
0.00%
发文量
34
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