国际监管使用急性系统性毒性数据,并整合新方法方法的方法
Judy Strickland1, Esther Haugabrooks2, David G Allen1
1Inotiv, Inc., Research Triangle Park, NC, USA.
Critical reviews in toxicology
|August 30, 2023
概括
世界各地的监管机构需要急性系统性毒性数据进行风险评估. 本次对国际替代试验方法合作组织 (ICATM) 成员国家的审查显示,对非动物替代品的接受程度有限,阻碍了进展.
科学领域:
- 毒理学 毒理学 毒理学
- 监管科学 监管科学
- 化学安全 化学安全
背景情况:
- 全球化学品监管机构要求急性全身毒性数据 (口腔,皮肤,吸入) 用于人类健康风险评估.
- 国际替代试验方法合作 (ICATM) 旨在推进非动物试验策略.
研究的目的:
- 审查ICATM成员管辖区的急性系统性毒性测试要求.
- 找出非动物替代方法用于急性毒性测试的监管接受的机会.
主要方法:
- 对巴西,加拿大,中国,欧盟,日本,韩国,台湾和美国的急性系统性毒性测试要求进行了全面审查.
- 该审查涵盖了各种化学部门,包括化品,消费品,工业化学品,药品,医疗器械和农药.
主要成果:
- 急性系统性毒性数据主要用于危险评估,分类和标签,在定量风险评估中使用较少.
- 虽然在动物试验是强制性的情况下,通常会推动物减少方法,但在许多司法管辖区和部门中,非动物替代品往往不被接受.
- 一些司法管辖区为减免试验提供指导,以减少在特定情况下使用动物.
结论:
- 了解急性系统性毒性测试的国际监管格局对于ICATM的非动物替代品的战略开发和实施至关重要.
- 需要进一步努力,以促进非动物替代品的接受和监管使用,以评估急性毒性危险和风险.
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