Literature DB >> 28666717

Drivers and barriers in the consistency approach for vaccine batch release testing: Report of an international workshop.

Martijn W P Bruysters1, Marie-Jeanne Schiffelers2, Marieke Hoonakker3, Carmen Jungbaeck4, Ian Ragan5, Eddy Rommel6, Ton van der Stappen7, Laura Viviani8, Ellen V Hessel9, Arnoud M Akkermans10, Rob J Vandebriel11.   

Abstract

Safety and potency assessment for batch release testing of established vaccines still relies partly on animal tests. An important avenue to move to batch release without animal testing is the consistency approach. This approach is based on thorough characterization of the vaccine, and the principle that the quality of subsequent batches is the consequence of the application of consistent production of batches monitored by a GMP quality system. Efforts to implement the consistency approach are supported by several drivers from industry, government, and research, but there are also several barriers that must be overcome. A workshop entitled "Consistency Approach, Drivers and Barriers" was organized, which aimed to discuss and identify drivers and barriers for the implementation of the 3Rs in the consistency approach from three different perspectives/domains (industry, regulatory and science frameworks). The workshop contributed to a better understanding of these drivers and barriers and resulted in recommendations to improve the overall regulatory processes for the consistency approach. With this report, we summarise the outcome of this workshop and intend to offer a constructive contribution to the international discussion on regulatory acceptance of the consistency approach.
Copyright © 2017 International Alliance for Biological Standardization. Published by Elsevier Ltd. All rights reserved.

Keywords:  3R; Barriers; Consistency approach; Drivers; Regulatory acceptance; Vaccine batch release

Mesh:

Substances:

Year:  2017        PMID: 28666717     DOI: 10.1016/j.biologicals.2017.06.006

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


  5 in total

1.  The Promises of Speeding Up: Changes in Requirements for Animal Studies and Alternatives during COVID-19 Vaccine Approval-A Case Study.

Authors:  Merel Ritskes-Hoitinga; Yari Barella; Tineke Kleinhout-Vliek
Journal:  Animals (Basel)       Date:  2022-07-05       Impact factor: 3.231

2.  Raman spectroscopy-based identification of toxoid vaccine products.

Authors:  Anja Silge; Thomas Bocklitz; Bjoern Becker; Walter Matheis; Juergen Popp; Isabelle Bekeredjian-Ding
Journal:  NPJ Vaccines       Date:  2018-10-04       Impact factor: 7.344

3.  Animal testing for vaccines. Implementing replacement, reduction and refinement: challenges and priorities.

Authors:  Arnoud Akkermans; Jean-Michel Chapsal; Eliana M Coccia; Hilde Depraetere; Jean-François Dierick; Parichat Duangkhae; Sunil Goel; Marlies Halder; Coenraad Hendriksen; Robin Levis; Koraphong Pinyosukhee; Dieter Pullirsch; Gautam Sanyal; Li Shi; Robert Sitrin; Dean Smith; Paul Stickings; Eriko Terao; Sylvie Uhlrich; Laura Viviani; Jim Webster
Journal:  Biologicals       Date:  2020-10-08       Impact factor: 1.856

4.  Degradomics-Based Analysis of Tetanus Toxoids as a Quality Control Assay.

Authors:  Thomas J M Michiels; Wichard Tilstra; Martin R J Hamzink; Justin W de Ridder; Maarten Danial; Hugo D Meiring; Gideon F A Kersten; Wim Jiskoot; Bernard Metz
Journal:  Vaccines (Basel)       Date:  2020-12-01

5.  Macrophage Activation Assays to Evaluate the Immunostimulatory Capacity of Avibacterium paragallinarum in A Multivalent Poultry Vaccine.

Authors:  Robin H G A van den Biggelaar; Willem van Eden; Victor P M G Rutten; Christine A Jansen
Journal:  Vaccines (Basel)       Date:  2020-11-10
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.