Literature DB >> 27546184

Introduction to the application of QbD principles for the development of monoclonal antibodies.

Christof Finkler1, Lynne Krummen2.   

Abstract

Quality by Design (QbD) is a global regulatory initiative with the goal of enhancing pharmaceutical development through the proactive design of pharmaceutical manufacturing process and controls to consistently deliver the intended performance of the product. The principles of pharmaceutical development relevant to QbD are described in the ICH guidance documents (ICHQ8-11). An integrated set of risk assessments and their related elements developed at Roche/Genentech were designed to provide an overview of product and process knowledge for the production of a recombinant monoclonal antibody. This chapter introduces a publication series on the application of Quality by Design for biopharmaceuticals, with a focus on the development of recombinant monoclonal antibodies. The development of and overview on the QbD concept applied by Roche and Genentech is described and essential QbD elements are presented.
Copyright © 2016 International Alliance for Biological Standardization. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Quality by Design

Mesh:

Substances:

Year:  2016        PMID: 27546184     DOI: 10.1016/j.biologicals.2016.07.004

Source DB:  PubMed          Journal:  Biologicals        ISSN: 1045-1056            Impact factor:   1.856


  6 in total

1.  Determination of Critical Quality Attributes for a Biotherapeutic in the QbD Paradigm: GCSF as a Case Study.

Authors:  Sumit K Singh; Deepak Kumar; Anurag S Rathore
Journal:  AAPS J       Date:  2017-09-05       Impact factor: 4.009

Review 2.  Molecular and functional analysis of monoclonal antibodies in support of biologics development.

Authors:  Xin Wang; Zhiqiang An; Wenxin Luo; Ningshao Xia; Qinjian Zhao
Journal:  Protein Cell       Date:  2017-07-21       Impact factor: 14.870

3.  A Quadrupole Dalton-based multi-attribute method for product characterization, process development, and quality control of therapeutic proteins.

Authors:  Weichen Xu; Rod Brian Jimenez; Rachel Mowery; Haibin Luo; Mingyan Cao; Nitin Agarwal; Irina Ramos; Xiangyang Wang; Jihong Wang
Journal:  MAbs       Date:  2017-08-14       Impact factor: 5.857

4.  Upstream cell culture process characterization and in-process control strategy development at pandemic speed.

Authors:  Jianlin Xu; Jianfa Ou; Kyle P McHugh; Michael C Borys; Anurag Khetan
Journal:  MAbs       Date:  2022 Jan-Dec       Impact factor: 5.857

5.  Quality by Design risk assessments supporting approved antibody products.

Authors:  Brian Kelley
Journal:  MAbs       Date:  2016-09-12       Impact factor: 5.857

Review 6.  Design Space and QbD Approach for Production of Drug Nanocrystals by Wet Media Milling Techniques.

Authors:  Leena Peltonen
Journal:  Pharmaceutics       Date:  2018-07-25       Impact factor: 6.321

  6 in total

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