Quality by Design (QbD) in Industrial Pharmacy: Enhancing Drug Development and Manufacturing Efficiency
Received Date: Aug 01, 2024 / Published Date: Aug 30, 2024
Abstract
Quality by Design (QbD) is a systematic approach to pharmaceutical development that emphasizes designing quality into processes from the outset rather than relying solely on end-product testing. In the field of Industrial Pharmacy, QbD is revolutionizing drug development and manufacturing by enhancing efficiency, reducing costs, and ensuring product quality. This article explores the principles of QbD, its application in drug development, and its impact on manufacturing efficiency. We discuss key elements such as critical quality attributes (CQAs), critical process parameters (CPPs), and the importance of risk management. Additionally, we examine case studies and the role of regulatory agencies in promoting QbD practices. The article concludes with insights into the future of QbD in Industrial Pharmacy, highlighting its potential to further transform the pharmaceutical industry.
Citation: Akhter C (2024) Quality by Design (QbD) in Industrial Pharmacy:Enhancing Drug Development and Manufacturing Efficiency. Int J Res Dev PharmL Sci, 10: 226.
Copyright: © 2024 Akhter C. 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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