Chapter 17. Industrial Continuous-flow Chemistry under cGMP Conditions

R. Moylan, S. Bourke, K. P. Cole, S. May
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引用次数: 3

Abstract

Adopting continuous manufacturing requires considerable upfront investment in technology and expertise to develop and execute robust processes. cGMP manufacturing control strategies for drug substance processes in particular are limited, with few real case studies available in the literature. Making the change from a traditional batch manufacturing paradigm to a new continuous paradigm can be highly disruptive. In this chapter, key enablers for running continuous processes including multi-step processes are presented. These enablers allow the process to run in a state of control such that the environmental, safety, quality and cost benefits associated with continuous processing may be realized. The enablers include the use of process analytical technology, a material tracking system, a diversion strategy and the incorporation of surge capacity. Examples from the field where these control strategy enablers were successfully used to produce drug substance API using continuous technology under cGMP conditions are also presented. In these case studies the environmental, safety and quality benefits realized are highlighted and the evolution of the technology from single step batch-continuous hybrid processes to multi-step fully continuous telescoped processes is described.
第十七章。cGMP条件下的工业连续流化学
采用连续制造需要在技术和专业知识方面进行大量的前期投资,以开发和执行稳健的流程。特别是原料药工艺的cGMP生产控制策略是有限的,文献中很少有真实的案例研究。从传统的批量生产模式到新的连续生产模式的转变可能是高度破坏性的。在本章中,介绍了运行连续过程(包括多步骤过程)的关键支持因素。这些使能器允许过程在受控状态下运行,从而实现与连续处理相关的环境、安全、质量和成本效益。这些推动因素包括过程分析技术的使用、材料跟踪系统、转移策略和浪涌容量的结合。还介绍了在cGMP条件下使用连续技术成功地将这些控制策略使能器用于生产原料药原料药的实例。在这些案例研究中,强调了所实现的环境、安全和质量效益,并描述了从单步分批-连续混合工艺到多步全连续伸缩工艺的技术演变。
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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