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Uncertainty-conscious methodology for process performance assessment in biopharmaceutical drug product manufacturing

机译:生物制药药品制造中工艺性能评估的不确定性意识方法

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This work presents an uncertainty-conscious methodology for the assessment of process performancefor example, run timein the manufacturing of biopharmaceutical drug products. The methodology is presented as an activity model using the type 0 integrated definition (IDEF0) functional modeling method, which systematically interconnects information, tools, and activities. In executing the methodology, a hybrid stochastic-deterministic model that can reflect operational uncertainty in the assessment result is developed using Monte Carlo simulation. This model is used in a stochastic global sensitivity analysis to identify tasks that had large impacts on process performance under the existing operational uncertainty. Other factors are considered, such as the feasibility of process modification based on Good Manufacturing Practice, and tasks to be improved is identified as the overall output. In a case study on cleaning and sterilization processes, suggestions were produced that could reduce the mean total run time of the processes by up to 40%. (c) 2017 American Institute of Chemical Engineers AIChE J, 64: 1272-1284, 2018
机译:这项工作提出了一种有意识的有意识的方法,用于评估流程性能,例如,在生物制药药品的制造中运行时滞。使用类型0集成定义(IDEF0)功能建模方法作为活动模型呈现该方法,其系统地互连信息,工具和活动。在执行方法中,使用Monte Carlo仿真开发了可以反映评估结果中运行不确定性的混合随机确定性模型。该模型用于随机全球敏感性分析,以确定在现有的运营不确定性下对过程性能影响大的任务。考虑了其他因素,例如基于良好制造实践的过程修改的可行性,以及要改进的任务被识别为整体输出。在清洁和灭菌过程的案例研究中,生产的建议可以将过程的平均总运行时间降低至40%。 (c)2017年美国化学工程师研究所Aiche J,64:1272-1284,2018

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