In Vitro Performance Tests for Continuous Manufacturing: The Impact on the Current Compendial Framework from the Viewpoint of the USP New Advancements in Product Performance Testing Expert Panel

IF 1 4区 医学 Q4 PHARMACOLOGY & PHARMACY Dissolution Technologies Pub Date : 2023-01-01 DOI:10.14227/dt300123p6
Hanlin Li, lshai Nir, Andre Hermans, R. Fahmy, Xujin Lu, Carrie A. Coutant
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引用次数: 3

Abstract

As continuous manufacturing (CM) evolves from an emerging to widely adopted technology by industry in drug product manufacturing, the compendiaI framework in product performance testing is also being evaluated for its applicability in CM. As such, the CM Working Group of the New Advancements in Product Performance Testing (NAPPT) Expert Panel was convened in 2019 to review the current standard for product performance testing, identify gaps in its applicability to CM, and recommend the development of new standards to support the adoption of advancing technologies industry-wide. This Stimuli article discusses the challenges and limitations of the current performance testing by dissolution for CM applications. It also presents recommendations on alternatives or surrogate methods, including in/at-line process analytical technology methods, with a decision tree to support users in identifying an option that is fit for their process. The Expert Panel seeks stakeholder feedback on the recommendations presented in this Stimuli article, and requests additional comments on the perceived challenges and limitations of performance testing.
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连续生产的体外性能测试:从USP产品性能测试专家小组的新进展的角度对现行药典框架的影响
随着连续生产(CM)从一种新兴技术发展到被药品制造行业广泛采用,产品性能测试中的药典框架也在评估其在连续生产中的适用性。因此,2019年召集了产品性能测试新进展(NAPPT)专家小组的CM工作组,审查当前的产品性能测试标准,确定其对CM适用性的差距,并建议制定新标准,以支持全行业采用先进技术。这篇刺激文章讨论了当前CM应用中溶解性性能测试的挑战和局限性。它还提出了关于替代方法或替代方法的建议,包括在线过程分析技术方法,以及一个决策树,以支持用户识别适合其过程的选项。专家小组寻求利益相关者对这篇刺激物文章中提出的建议的反馈,并要求对性能测试的挑战和局限性提出更多的意见。
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来源期刊
Dissolution Technologies
Dissolution Technologies 医学-药学
CiteScore
1.20
自引率
33.30%
发文量
14
审稿时长
3 months
期刊介绍: Dissolution Technologies is a peer reviewed quarterly publication reporting ongoing, useful information on dissolution testing of pharmaceuticals. It provides an international forum for dissolution analysts to receive and exchange information on various dissolution topics. Dissolution Technologies welcomes submissions related to dissolution, in vitro release, and disintegration testing. These topics should be the major focus of the article. Do not submit articles where the focus is formulation development with dissolution testing as one of many tests.
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