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

Other Titles
Quality by Design (QbD) application for the pharmaceutical development process
Authors
Lee, Sang-HoKim, Jin-KiJee, Jun-PilJang, Dong-JinPark, Young-JoonKim, Joo-Eun
Issue Date
Nov-2022
Publisher
한국약제학회
Keywords
Quality by Design; Pharmaceutical development process; QTPP; CQAs; CMAs; CPPs
Citation
Journal of Pharmaceutical Investigation, v.52, no.6, pp 649 - 682
Pages
34
Indexed
SCIE
SCOPUS
KCI
Journal Title
Journal of Pharmaceutical Investigation
Volume
52
Number
6
Start Page
649
End Page
682
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/111473
DOI
10.1007/s40005-022-00575-x
ISSN
2093-5552
2093-6214
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.
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