Report of the European Commission workshop on “The roadmap towards phasing out animal testing for chemical safety assessments”, Brussels, 11–12 December 2023

IF 3.5 4区 医学 Q1 MEDICINE, LEGAL Regulatory Toxicology and Pharmacology Pub Date : 2025-04-04 DOI:10.1016/j.yrtph.2025.105818
Mark T.D. Cronin , Elisabet Berggren , Sofia Camorani , Christian Desaintes , Marco Fabbri , Julia Fabrega , Matthias Herzler , Jay D.E. Ingram , Katia Lacasse , Susanna Louhimies , Gavin Maxwell , Katrin Schutte , Tomasz Sobanski , Georg Streck , Andrea Terron , Andrew P. Worth
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Abstract

This report summarises the main findings and discussion from the European Commission (EC) workshop on “The Roadmap Towards Phasing Out Animal Testing for Chemical Safety Assessments” which was held in Brussels on 11–12 December 2023. The aim of the workshop was to gather ideas and opinions from individuals, organisations and institutions, and to discuss potential approaches for incorporating non-animal methods into chemical legislation with all interested stakeholders. The roadmap will be an EC policy document which will outline milestones and specific actions, addressing all relevant pieces of chemical legislation relating to safety assessment. It intends to describe the necessary steps to replace animal testing in pieces of legislation where it is currently required for chemical safety assessments. The roadmap will outline the path to expand and accelerate the development, validation and implementation of non-animal methods as well as means to facilitate their uptake across legislation. The workshop included presentations from a wide variety of stakeholders. The contributors provided examples of how non-animal methods could be applied to replace, reduce or refine animal testing in the assessment of human health and environmental effects. Furthermore, possible guiding principles for establishing a Next-Generation Risk Assessment (NGRA) in European chemicals legislation were also discussed. The workshop provided the basis for further discussion and for structuring the roadmap work.

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欧盟委员会关于“逐步淘汰化学安全评估动物试验路线图”的研讨会报告,布鲁塞尔,2023年12月11日至12日。
本报告总结了欧盟委员会(EC)于2023年12月11日至12日在布鲁塞尔举行的“逐步淘汰化学安全评估动物试验路线图”研讨会的主要发现和讨论。研讨会的目的是收集个人、组织和机构的想法和意见,并与所有感兴趣的利益相关者讨论将非动物方法纳入化学品立法的潜在方法。该路线图将是一份欧盟政策文件,将概述里程碑和具体行动,解决与安全评估有关的所有相关化学品立法。它打算描述必要的步骤,以取代动物试验的立法部分,目前需要进行化学安全评估。该路线图将概述扩大和加速非动物方法的开发、验证和实施的途径,以及促进其在立法中采用的手段。研讨会包括来自各种利益相关者的演讲和讨论。提交者提供了一些例子,说明在评估人类健康和环境影响时如何应用非动物方法来取代、减少或改进动物试验。此外,还讨论了在欧洲化学品立法中建立下一代风险评估(NGRA)的可能指导原则。讲习班为进一步讨论和组织进一步的路线图工作提供了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.70
自引率
8.80%
发文量
147
审稿时长
58 days
期刊介绍: Regulatory Toxicology and Pharmacology publishes peer reviewed articles that involve the generation, evaluation, and interpretation of experimental animal and human data that are of direct importance and relevance for regulatory authorities with respect to toxicological and pharmacological regulations in society. All peer-reviewed articles that are published should be devoted to improve the protection of human health and environment. Reviews and discussions are welcomed that address legal and/or regulatory decisions with respect to risk assessment and management of toxicological and pharmacological compounds on a scientific basis. It addresses an international readership of scientists, risk assessors and managers, and other professionals active in the field of human and environmental health. Types of peer-reviewed articles published: -Original research articles of relevance for regulatory aspects covering aspects including, but not limited to: 1.Factors influencing human sensitivity 2.Exposure science related to risk assessment 3.Alternative toxicological test methods 4.Frameworks for evaluation and integration of data in regulatory evaluations 5.Harmonization across regulatory agencies 6.Read-across methods and evaluations -Contemporary Reviews on policy related Research issues -Letters to the Editor -Guest Editorials (by Invitation)
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