Jenzsch Marco, Bell Christian, Buziol Stefan, Kepert Felix, Wegele Harald, Hakemeyer Christian
Roche Pharma Technical Operations - Biologics Manufacturing, Nonnenwald 2, 82377, Penzberg, Germany.
Roche Pharma Technical Operations - Biologics Analytical Development Europe, Grenzacherstrasse 124, 4070, Basel, Switzerland.
Adv Biochem Eng Biotechnol. 2018;165:211-252. doi: 10.1007/10_2017_18.
Process analytical technology (PAT), the regulatory initiative for incorporating quality in pharmaceutical manufacturing, is an area of intense research and interest. If PAT is effectively applied to bioprocesses, this can increase process understanding and control, and mitigate the risk from substandard drug products to both manufacturer and patient. To optimize the benefits of PAT, the entire PAT framework must be considered and each elements of PAT must be carefully selected, including sensor and analytical technology, data analysis techniques, control strategies and algorithms, and process optimization routines. This chapter discusses the current state of PAT in the biopharmaceutical industry, including several case studies demonstrating the degree of maturity of various PAT tools. Graphical Abstract Hierarchy of QbD components.
过程分析技术(PAT)作为制药生产中融入质量理念的监管举措,是一个备受关注且研究活跃的领域。如果将PAT有效地应用于生物过程,就能增进对过程的理解与控制,并降低不合格药品给制造商和患者带来的风险。为了优化PAT的效益,必须考虑整个PAT框架,且要精心挑选PAT的各个要素,包括传感器和分析技术、数据分析技术、控制策略与算法以及过程优化程序。本章讨论了生物制药行业中PAT的现状,包括若干案例研究,展示了各种PAT工具的成熟程度。图形摘要:质量源于设计(QbD)组件的层次结构。