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Quality by Design (QbD) application for the pharmaceutical development process

Title
Quality by Design (QbD) application for the pharmaceutical development process
Other Titles
Quality by Design (QbD) application for the pharmaceutical development process
Author
김진기
Keywords
Quality by Design; Pharmaceutical development process; QTPP; CQAs; CMAs; CPPs
Issue Date
2022-08
Publisher
SPRINGERNATURE
Citation
JOURNAL OF PHARMACEUTICAL INVESTIGATION, v. 52.0, NO. 6, Page. 649-682
Abstract
Background Quality by Design (QbD) is a pharmaceutical quality management system that predicts, controls, and systematically responds to risks that may occur in the research stage and manufacturing process. There are many articles on how to improve quality through application of the QbD system, but the methodology surrounding how to specifically apply this process is limited. The purpose of this review was to provide accurate information on drug development process and overcome the difficulties of developing QbD-applied drug products through an appropriate application method. Area covered QbD-based pharmaceuticals are continuously being developed worldwide, helping to identify potential risks, and managing all aspects, from drug design to patient consumption, further enabling the patient to be administered a high-quality drugs based on their design. In this study, a basic knowledge of QbD, its application and effectiveness during drug development will be discussed. Expert opinion Our results suggest that a QbD for drug development can reduce risk to patients, improve drug quality, and continuously produce superior quality drug products.
URI
https://link.springer.com/article/10.1007/s40005-022-00575-xhttps://repository.hanyang.ac.kr/handle/20.500.11754/179274
ISSN
2093-5552;2093-6214
DOI
10.1007/s40005-022-00575-x
Appears in Collections:
COLLEGE OF PHARMACY[E](약학대학) > PHARMACY(약학과) > Articles
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