| Literature DB >> 25980924 |
Christoph Herwig1, Oscar F Garcia-Aponte2, Aydin Golabgir3, Anurag S Rathore4.
Abstract
In the quality by design (QbD) paradigm, global regulatory agencies have introduced the concepts of quality risk management and knowledge management (KM) as enablers for an enhanced pharmaceutical quality system. Although the concept of quality risk management has been well elucidated in the literature, the topic of KM has received relatively scant attention. In this paper we present an opinion on KM in the QbD paradigm as it relates to the manufacturing of biotech therapeutic products. Both academic and industrial viewpoints have been considered and key gaps have been elucidated. The authors conclude that there is an urgent need for the biotech industry to create efficient KM approaches if they wish to be successful in QbD implementation.Keywords: bioprocessing; knowledge management; quality by design
Mesh:
Year: 2015 PMID: 25980924 DOI: 10.1016/j.tibtech.2015.04.004
Source DB: PubMed Journal: Trends Biotechnol ISSN: 0167-7799 Impact factor: 19.536