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Characteristics of the U.S. EPAs Office of Pesticide Programs toxicity information databases.

机译:美国EPA农药计划办公室的毒性信息数据库的特征。

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摘要

The United States Environmental Protection Agency's Office of Pesticide Programs (OPP) requires that data from toxicity testing be submitted to the OPP to support the registration of pesticide chemicals. Once the toxicity data are submitted, they are entered into various toxicity databases. The studies are listed in an archival database to catalog and allow retrieval of the study for review. Reviews of toxicity studies are then placed into a separate database that can be retrieved to support a regulatory position. Toxicity information for health effects other than cancer and gene mutations from chronic exposure is reviewed through a reference dose (RfD) approach, and these decisions and supporting data are entered into an RfD database. Carcinogenicity data are reviewed by a peer review process, and these decisions are entered into a newly developed database to show the regulatory decision with supporting data. The mutagenicity data are reviewed and acceptable data are entered into the Genetic Activity Profile system to catalog and display the submitted information. These databases contain the information used for hazard evaluations as part of the OPP review of pesticide chemicals.
机译:美国环境保护局的农药计划办公室(OPP)要求将毒性试验的数据提交给OPP,以支持农药化学物质的注册。提交毒性数据后,将其输入到各种毒性数据库中。这些研究会在档案数据库中列出,以进行分类并允许检索研究以进行审查。然后将毒性研究的评论放到一个单独的数据库中,可以检索该数据库来支持法规立场。通过参考剂量(RfD)方法审查癌症和慢性暴露引起的基因突变以外的健康影响的毒性信息,并将这些决定和支持数据输入RfD数据库。致癌性数据由同行评审过程进行评审,并将这些决策输入到新开发的数据库中,以显示具有支持数据的监管决策。审查诱变性数据,并将可接受的数据输入到遗传活性谱系统中,以分类并显示提交的信息。这些数据库包含用于农药评估OPP审查的危害评估信息。

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