Aug 2026· Regulatory toxicology and pharmacology : RTP· Vol 172, pp.
106222
· 0 citations· 28 references
Medicine
Abstract
Acute oral toxicity (AOT) testing is widely used for hazard identification in chemical safety assessment, but traditional animal methods are still implemented despite their scientific limitations and ethical implications. Despite the availability of non-animal methods, regulatory uptake has been inconsistent, also due to a lack of structured guidance. To address this, the Animal-Free Safety Assessment Collaboration has developed a science-based Decision Tree (DT) aligned with the Organisation for Economic Cooperation and Development (OECD) Integrated Approaches to Testing and Assessment (IATA) framework. IATA integrate existing information in a Weight of Evidence (WoE) assessment with the possible generation of new data appropriate to the decision context. The DT is built as a specific IATA to provide a transparent, modular workflow integrating in silico tools, in vitro assays, and WoE strategies to support AOT hazard identification for regulatory decision-making, such as European Union's Registration, Evaluation, Authorisation, and Restriction of Chemicals (REACH) Regulation, ensuring that animal testing is used only as a last resort. The DT aims to inform regulatory guidance updates and promote acceptance of non-animal approaches by formalising decision-making to bridge the gap between legal mandates to reduce animal testing and current regulatory practice, still heavily reliant on animals, supporting the transition toward improved chemical safety evaluations.
The evaluation of 28- and 90-day repeated-dose toxicity studies in rodents is typically performed at the highest tier of regulatory toxicology. Despite detailed guidance from the European Food Safety Authority (EFSA) and Organisation for Economic Co-operation and Development (OECD), the practical implementation and eva...
S. Favilla, Eugenio Traini, M. Ardizzone et al.· Regulatory toxicology and ph...· 0 citations
Five key recommendations for future health risk assessments are concluded, prioritizing PFAS; improving analytical methods; promoting generation of robust data and data gap filling; promoting open science, including the development of shared data infrastructure and cross-institutional knowledge exchange; and strengthen...
J. Kowalczyk, Klaus Abraham, Christina August et al.· Archives of Toxicology· 0 citations
The European Union (EU) Registration, Evaluation, Authorisation and Restriction of Chemicals Regulation (EC No. 1907/2006) (REACH) includes the principle of testing only when scientifically necessary, integrating mechanisms for data sharing, read-across, and adaptations to minimise vertebrate animal testing. REACH alre...
M. van Velthoven, G. Pallocca, Vicente Aranda et al.· Regulatory toxicology and ph...· 1 citation
The increasing proliferation of policy-driven frameworks addressing chemical safety and sustainability has intensified the need for coherence and integration in environmental assessment and management. In the European context, Safe and Sustainable by Design (SSbD) and the EU Ecolabel represent influential but conceptua...
Arthur Ribas de Souza Sales· Integrated Environmental Ass...· 0 citations
The "Safe and Sustainable by Design" (SSbD) approach promotes the development of chemicals that are inherently safer and more sustainable, including viable alternatives to hazardous substances. It involves assessing the toxicity, environmental impact and functionality of potential substitutes to ensure that they meet p...
Karolina Jagiello, Szymon Zdybel, A. Sosnowska et al.· Environment International· 0 citations
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