Literature DB >> 24598725

Implementation of QbD for the development of a vaccine candidate.

Jennifer Haas1, Andrew Franklin2, Matthew Houser2, David Maraldo3, Mark Mikola2, Roberto Ortiz2, Elizabeth Sullivan2, José M Otero3.   

Abstract

This case study provides an example of how Quality by Design (QbD) principles were applied to accelerate process development to manufacture a vaccine candidate at commercial scale. By leveraging an existing manufacturing platform process, a risk assessment was used to differentiate process parameters that could be defined using a combination of scientific and historical manufacturing knowledge from those that merited additional process characterization by experimentation. Select parameters, and their interactions, were evaluated by a Design of Experiment (DoE) series. This systematic approach required less time and fewer resources and resulted in the definition of a reliable and robust manufacturing process that meets regulatory requirements.
Copyright © 2014 Elsevier Ltd. All rights reserved.

Keywords:  FMEA; Process development; Quality by Design; Vaccines

Mesh:

Substances:

Year:  2014        PMID: 24598725     DOI: 10.1016/j.vaccine.2014.02.028

Source DB:  PubMed          Journal:  Vaccine        ISSN: 0264-410X            Impact factor:   3.641


  2 in total

Review 1.  Developments in the formulation and delivery of spray dried vaccines.

Authors:  Gaurav Kanojia; Rimko Ten Have; Peter C Soema; Henderik Frijlink; Jean-Pierre Amorij; Gideon Kersten
Journal:  Hum Vaccin Immunother       Date:  2017-10-03       Impact factor: 3.452

2.  Quality by Design Micro-Engineering Optimisation of NSAID-Loaded Electrospun Fibrous Patches.

Authors:  Kazem Nazari; Prina Mehta; Muhammad Sohail Arshad; Shahabuddin Ahmed; Eleftherios G Andriotis; Neenu Singh; Omar Qutachi; Ming-Wei Chang; Dimitrios G Fatouros; Zeeshan Ahmad
Journal:  Pharmaceutics       Date:  2019-12-18       Impact factor: 6.321

  2 in total

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