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Application of omics data in regulatory toxicology: report of an international BfR expert workshop

机译:组学数据在法规毒理学中的应用:国际BfR专家研讨会的报告

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摘要

Advances in omics techniques and molecular toxicology are necessary to provide new perspectives for regulatory toxicology. By the application of modern molecular techniques, more mechanistic information should be gained to support standard toxicity studies and to contribute to a reduction and refinement of animal experiments required for certain regulatory purposes. The relevance and applicability of data obtained by omics methods to regulatory purposes such as grouping of chemicals, mode of action analysis or classification and labelling needs further improvement, defined validation and cautious expert judgment. Based on the results of an international expert workshop organized 2014 by the Federal Institute for Risk Assessment in Berlin, this paper is aimed to provide a critical overview of the regulatory relevance and reliability of omics methods, basic requirements on data quality and validation, as well as regulatory criteria to decide which effects observed by omics methods should be considered adverse or non-adverse. As a way forward, it was concluded that the inclusion of omics data can facilitate a more flexible approach for regulatory risk assessment and may help to reduce or refine animal testing.
机译:组学技术和分子毒理学的进步对于为调节毒理学提供新的观点是必要的。通过应用现代分子技术,应该获得更多的机械信息,以支持标准毒性研究,并有助于减少和完善某些监管目的所需的动物实验。通过组学方法获得的数据与法规目的(如化学品分组,作用模式分析或分类和标签)的相关性和适用性需要进一步改进,确定的验证和谨慎的专家判断。基于2014年柏林联邦风险评估研究所组织的一次国际专家研讨会的结果,本白皮书旨在提供对组学方法的监管相关性和可靠性,数据质量和验证的基本要求以及其他方面的重要概述。作为决定是否应通过组学方法观察到的不良反应或不良反应的管理标准。作为前进的方向,得出的结论是,包含组学数据可以促进监管风险评估的更灵活方法,并且可以帮助减少或改进动物试验。

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