Enhancing Pharmaceutical Manufacturing through Process Analytical Technology
Received Date: Mar 01, 2025 / Published Date: Mar 28, 2025
Abstract
Process Analytical Technology (PAT) is a framework established by the U.S. Food and Drug Administration to design, analyze, and control manufacturing processes through timely measurements of critical quality and performance attributes. PAT enhances process understanding and enables real-time monitoring and control, leading to increased efficiency, reduced variability, and enhanced product quality. It is especially impactful in pharmaceutical and fine chemical manufacturing, where compliance with strict quality regulations is essential. This article explores PAT tools, implementation strategies, and its integration with automation and continuous manufacturing systems.
Citation: Wei-Lin Z (2025) Enhancing Pharmaceutical Manufacturing throughProcess Analytical Technology. J Mol Pharm Org Process Res 13: 281.
Copyright: 漏 2025 Wei-Lin Z. This is an open-access article distributed under theterms of the Creative Commons Attribution License, which permits unrestricteduse, distribution, and reproduction in any medium, provided the original author andsource are credited.
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