• <noscript id="eccgc"></noscript><noscript id="eccgc"><kbd id="eccgc"></kbd></noscript>
  • Full-Text Search:
    Home|Journal Papers|About CNKI|User Service|FAQ|Contact Us|中文
    《亚洲药物制剂科学(英文版)》 2017-01
    Add to Favorite Get Latest Update

    Application of quality by design in the current drug development

    Lan Zhang;Shirui Mao;Shenyang Pharmaceutical University;  
    Quality by Test was the only way to guarantee quality of drug products before FDA launched current Good Manufacturing Practice. To clearly understand the manufacture processes, FDA generalized Quality by Design(QbD) in the field of pharmacy, which is based on the thorough understanding of how materials and process parameters affect the quality profile of final products. The application of QbD in drug formulation and process design is based on a good understanding of the sources of variability and the manufacture process. In this paper,the basic knowledge of QbD, the elements of QbD, steps and tools for QbD implementation in pharmaceutics field, including risk assessment, design of experiment, and process analytical technology(PAT), are introduced briefly. Moreover, the concrete applications of QbD in various pharmaceutical related unit operations are summarized and presented.
    【Fund】: financially supported by Talents Project of Liaoning Province China (LR2013047)
    【CateGory Index】: R95
    Download(CAJ format) Download(PDF format)
    CAJViewer7.0 supports all the CNKI file formats; AdobeReader only supports the PDF format.
    ?2006 Tsinghua Tongfang Knowledge Network Technology Co., Ltd.(Beijing)(TTKN) All rights reserved