Overcoming scientific barriers in the transition from in vivo to non-animal batch testing of human and veterinary vaccines

Author:

van den Biggelaar Robin H. G. A.1ORCID,Hoefnagel Marcel H.N.2ORCID,Vandebriel Rob J.3ORCID,Sloots Arjen4,Hendriksen Coenraad F.M.4,van Eden Willem1ORCID,Rutten Victor P. M. G.15ORCID,Jansen Christine A.16ORCID

Affiliation:

1. Division of Infectious Diseases and Immunology, Department of Biomolecular Health Sciences, Faculty of Veterinary Medicine, Utrecht University, Utrecht, The Netherlands

2. Quality Department, Medicines Evaluation Board, Utrecht, The Netherlands

3. Centre for Health Protection, National Institute for Public Health and the Environment (RIVM), Bilthoven, The Netherlands

4. Intravacc (Institute for Translational Vaccinology), Bilthoven, The Netherlands

5. Department of Veterinary Tropical Diseases, Faculty of Veterinary Science, University of Pretoria, Pretoria, South Africa

6. Cell Biology and Immunology Group, Department of Animal Sciences, Wageningen University and Research, Wageningen, The Netherlands

Funder

the Dutch Ministry of Agriculture, Nature and Food Quality, and the National Institute of Public Health & the Environment

the Dutch Ministry of Agriculture, Nature and Food Quality, and Intravacc

Publisher

Informa UK Limited

Subject

Drug Discovery,Pharmacology,Molecular Medicine,Immunology

Reference129 articles.

1. From empiricism to rational design: a personal perspective of the evolution of vaccine development

2. Vaccine quality—can a single standard be defined?

3. Commission to the European Parliament and the Council. 2019 Report on the Statistics on the Use of Animals for Scientific Purposes in the Member States of the European Union in 2015-2017. 2020.

4. Milne C, Buchheit KH. EDQM’s 3R activities in the field of quality control of vaccines. ALTEX. 2012;1/12.

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