Validation and quality control of replacement alternatives - current status and future challenges
Abstract
Abstract Alternatives to animal testing have been developed mainly in the fields of toxicology and vaccine testing. Typical examples are the evaluation of phototoxicity, eye irritation or skin corrosion/irritation of cosmetics and industrial chemicals. However, examples can also be found in other biomedical areas, such the control of the quality of drug preparations for pyrogens or for the control of the production process of biologics, such as botulinum neurotoxin. For regulatory purposes, the quality, transferability and predictivity of an alternative method needs to be evaluated. This procedure is called the “validation process” of a new method. It follows defined rules, and several governmental institutions have been established to perform, supervise or advise on this process. As this often results in a delay of method implementation, different alternatives for the evaluation of a method's suitability and quality are under discussion. We describe here the principles of model development and quality control. We also give an overview on methods that have undergone validation. Strengths and shortcomings of traditional approaches are discussed, and new developments and challenges are outlined.
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The regulatory use of in vitro methods has brought about the concepts that feed into validation.
“The regulatory use of in vitro methods has brought about the concepts that feed into validation (Leist et al., 2012).”
From Toward good in vitro reporting standards (2019) · cites this paper as Leist et al., 2012
Mechanistic validation may provide a measure of test method performance even when a good reference dataset is not available.
“Such an approach may provide a measure of test method performance, even when a good reference dataset is not available (Leist et al., 2012; Patlewicz et al., 2013; Patterson et al., 2021; Tigges et al., 2021).”
From Recommendations on fit-for-purpose criteria to establish quality management for microphysiological systems and for monitoring their reproducibility (2024) · cites this paper as Leist et al., 2012
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References 152 · Cited by 100
- Authors
- Leist, M., Hasiwa, N., Daneshian, M., & Hartung, T.
- Affiliations
- University of Konstanz (DE)
- Doerenkamp-Zbinden Chair for In-vitro Toxicology and Biomedicine and Center for Alternatives to Animal Testing in Europe (CAAT-Europe), University of Konstanz, D-78467 Konstanz, Germany
- Corresponding author
- Leist, Marcel
- ORCID
- Leist, Marcel
- Venue
- Toxicology Research
- Publisher
- Oxford University Press (OUP)
- Published
- 2012-05-28
- Volume
- 1
- Issue
- 1
- Pages
- 8-22
- ISSN
- 2045-452X (ISSN-L)
- 2045-4538
- OpenAlex
- W2016164331
- Cited by
- 100
- References
- 152
- Citations by year
- 2026: 6 · 2025: 2 · 2024: 10 · 2023: 6 · 2022: 4 · 2021: 1 · 2020: 3 · 2019: 8 · 2018: 12 · 2017: 6 · 2016: 7 · 2015: 6 · 2014: 14 · 2013: 10 · 2012: 5
- FWCI
- 16.19
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model (vor)
- Locations
- Toxicology Research (publishedVersion)
- KOPS (University of Konstanz) (submittedVersion)
- Topics
- Health Sciences › Veterinary › Small Animals › Animal testing and alternatives
- Life Sciences › Immunology and Microbiology › Immunology › Immunotoxicology and immune responses
- Physical Sciences › Chemistry › Analytical Chemistry › Analytical Methods in Pharmaceuticals
- Keywords
- alternatives to animal testing, method validation, quality control, phototoxicity testing, eye irritation, pyrogen testing, botulinum toxin, regulatory validation, model development
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