对欧洲非人类灵长类动物试验的意见

Q3 Pharmacology, Toxicology and Pharmaceutics
Michelle M. Epstein , Theo Vermeire
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引用次数: 3

摘要

健康、环境和新兴风险科学委员会(SCHEER)响应了欧盟委员会关于“在生物医学研究、产品和设备的生产和测试中需要非人类灵长类动物”的授权。现概述本意见。《意见》侧重于在以下领域的科学实验中取代、减少和改进使用非人类灵长类动物的方法:1)药品和医疗装置的开发和安全测试;2)传染病的治疗和预防;3)神经科学;4)眼科和5)(异种)移植。虽然无法预测欧洲国家卫生保健服务的使用将在多长时间内被淘汰,但《意见》总结了研究差距,并提出了诸如替代方法、培训、改进技术和规程、分享知识和消除障碍等建议。最后,提出了研究需求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An Opinion on non-human primates testing in Europe

The Scientific Committee on Health, Environmental and Emerging Risks (SCHEER) responded to a mandate from the European Commission on ‘The need for non-human primates in biomedical research, production and testing of products and devices’. An overview of this Opinion is presented. The Opinion focuses on the approaches aimed at the replacement, reduction and refinement (3Rs) of the use of non-human primates in scientific experimentation in the areas of 1) development and safety testing of pharmaceuticals and medical devices, 2) treatment and prevention of infectious diseases, 3) neuroscience, 4) ophthalmology and 5) (xeno)transplantation. While it is not possible to predict how long it will be before the use of NHPs in Europe are phased-out, the Opinion summarizes the research gaps and provides recommendations such as alternative methods, training, improvement of techniques and protocols, sharing of knowledge and removal of barriers. Finally, research needs are given.

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来源期刊
Drug Discovery Today: Disease Models
Drug Discovery Today: Disease Models Pharmacology, Toxicology and Pharmaceutics-Drug Discovery
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期刊介绍: Drug Discovery Today: Disease Models discusses the non-human experimental models through which inference is drawn regarding the molecular aetiology and pathogenesis of human disease. It provides critical analysis and evaluation of which models can genuinely inform the research community about the direct process of human disease, those which may have value in basic toxicology, and those which are simply designed for effective expression and raw characterisation.
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