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A review of human biomonitoring data used in regulatory risk assessment under Canada's Chemicals Management Program

机译:根据加拿大化学品管理计划,对用于法规风险评估的人类生物监测数据进行了审查

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摘要

As a part of the Chemicals Management Plan launched in 2006, the Government of Canada is assessing and managing, where appropriate, the potential health and ecological risks associated with approximately 4300 substances under the Canadian Environmental Protection Act (1999). Since that time, nearly 3000 substances have been assessed, with human biomonitoring (HBM) data playing an increasingly important role for some substances. Case studies are presented, including both inorganic and organic substances (i.e., selenium, triclosan, phthalates), which highlight the impact and overall role HBM has had in regulatory decision making in Canada for these three substances as well as criteria used in the application of HBM data in human health risk assessment. An overview of its limitations in terms of how and when HBM data can be applied, when assessing human health in a regulatory setting, is discussed as well as the role HBM data can play in priority setting. Crown Copyright (C) 2016 Published by Elsevier GmbH. All rights reserved.
机译:作为2006年启动的化学品管理计划的一部分,加拿大政府正在根据加拿大《环境保护法》(1999年),酌情评估和管理与大约4300种物质相关的潜在健康和生态风险。自那时以来,已经评估了近3000种物质,人类生物监测(HBM)数据对于某些物质起着越来越重要的作用。介绍了案例研究,包括无机和有机物质(即硒,三氯生,邻苯二甲酸盐),这些研究突显了HBM在加拿大针对这三种物质的监管决策中所产生的影响和总体作用,以及应用这些物质所采用的标准。人类健康风险评估中的HBM数据。讨论了在管理环境中评估人体健康时如何应用和何时应用HBM数据的局限性概述,以及HBM数据在优先级设置中可以发挥的作用。 Crown版权所有(C)2016,由Elsevier GmbH发布。版权所有。

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