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Meeting Report: Validation of Toxicogenomics-Based Test Systems: ECVAM–ICCVAM/NICEATM Considerations for Regulatory Use

机译:会议报告:基于毒物基因组学的测试系统的验证:ECVAM–ICCVAM / NICEATM法规使用注意事项

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摘要

This is the report of the first workshop “Validation of Toxicogenomics-Based Test Systems” held 11–12 December 2003 in Ispra, Italy. The workshop was hosted by the European Centre for the Validation of Alternative Methods (ECVAM) and organized jointly by ECVAM, the U.S. Interagency Coordinating Committee on the Validation of Alternative Methods (ICCVAM), and the National Toxicology Program (NTP) Interagency Center for the Evaluation of Alternative Toxicological Methods (NICEATM). The primary aim of the workshop was for participants to discuss and define principles applicable to the validation of toxicogenomics platforms as well as validation of specific toxicologic test methods that incorporate toxicogenomics technologies. The workshop was viewed as an opportunity for initiating a dialogue between technologic experts, regulators, and the principal validation bodies and for identifying those factors to which the validation process would be applicable. It was felt that to do so now, as the technology is evolving and associated challenges are identified, would be a basis for the future validation of the technology when it reaches the appropriate stage. Because of the complexity of the issue, different aspects of the validation of toxicogenomics-based test methods were covered. The three focus areas include a) biologic validation of toxicogenomics-based test methods for regulatory decision making, b) technical and bioinformatics aspects related to validation, and c) validation issues as they relate to regulatory acceptance and use of toxicogenomics-based test methods. In this report we summarize the discussions and describe in detail the recommendations for future direction and priorities.
机译:这是2003年12月11日至12日在意大利伊斯普拉举行的首个研讨会“基于毒物基因组学的测试系统验证”的报告。该研讨会由欧洲替代方法验证中心(ECVAM)主持,由ECVAM,美国替代方法验证机构间协调委员会(ICCVAM)和美国国家毒理学计划(NTP)机构间中心联合举办。评估其他毒理学方法(NICEATM)。讲习班的主要目的是让参加者讨论和定义适用于毒理基因组学平台验证以及采用毒理基因组学技术的特定毒理学测试方法验证的原理。研讨会被认为是在技术专家,监管机构和主要验证机构之间进行对话并确定可适用验证程序的因素的机会。人们认为,随着技术的发展以及相关挑战的确定,现在就这样做,将成为该技术达到适当阶段时未来进行验证的基础。由于问题的复杂性,涵盖了基于毒理基因组学的测试方法验证的不同方面。这三个重点领域包括:a)对基于遗传基因组学的测试方法进行监管决策的生物验证; b)与验证相关的技术和生物信息学方面;以及c)与监管机构接受和基于毒素基因组学的测试方法相关的验证问题。在本报告中,我们总结了讨论并详细描述了有关未来方向和优先事项的建议。

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