评论:通过风险科学积累非杀伤人员地雷知识。

IF 3 4区 医学 Q1 MEDICINE, LEGAL Regulatory Toxicology and Pharmacology Pub Date : 2024-09-16 DOI:10.1016/j.yrtph.2024.105702
Yadvinder Bhuller , Morgan Gale , Fevrelyn Yadao , Daniel Krewski
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引用次数: 0

摘要

第十二届世界生命科学替代品和动物使用大会为动员和交流有关科技进步的知识提供了一个平台。大会还为专家们提供了一个讨论如何加快采用新战略和新工具的机会。其中一项建议主张,有必要缩小尚未了解 "新方法"(NAMs)的下一代科学家与率先开发和验证这些非动物毒理学风险评估方法的当代思想领袖之间的差距。因此,在加拿大渥太华大学为 13 至 16 岁有兴趣了解风险科学以及如何利用 NAMs 为人类健康风险评估提供信息的学生开设了一门小型课程。该课程也是创建本文所提供的虚拟培训路线图的平台,从而将这一知识带给更多正在风险科学领域开创事业的学习者。
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Building knowledge of NAMs through risk science
The 12th World Congress on Alternatives and Animal Use in the Life Sciences provided a platform for mobilizing and exchanging knowledge on the advancements in science and technology. It also provided an opportunity for experts to discuss how to accelerate the adoption of new strategies and tools. One of these recommendations advocated the need to bridge the gap between the next generation of scientists who have yet to learn about ‘New Approach Methodologies’ (NAMs) and the current generation of thought leaders who have pioneered the development and validation of these non-animal approaches to toxicological risk assessment. Consequently, a mini-course, held at Canada's University of Ottawa, was developed for students, aged 13–16 years, interested in learning about risk science and how NAMs can be used to inform human health risk assessment. This course also served as a platform for creating a virtual training roadmap, provided in this paper, thereby bringing this knowledge to a broader audience of learners who are establishing their careers in the field of risk science.
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来源期刊
CiteScore
6.70
自引率
8.80%
发文量
147
审稿时长
58 days
期刊介绍: Regulatory Toxicology and Pharmacology publishes peer reviewed articles that involve the generation, evaluation, and interpretation of experimental animal and human data that are of direct importance and relevance for regulatory authorities with respect to toxicological and pharmacological regulations in society. All peer-reviewed articles that are published should be devoted to improve the protection of human health and environment. Reviews and discussions are welcomed that address legal and/or regulatory decisions with respect to risk assessment and management of toxicological and pharmacological compounds on a scientific basis. It addresses an international readership of scientists, risk assessors and managers, and other professionals active in the field of human and environmental health. Types of peer-reviewed articles published: -Original research articles of relevance for regulatory aspects covering aspects including, but not limited to: 1.Factors influencing human sensitivity 2.Exposure science related to risk assessment 3.Alternative toxicological test methods 4.Frameworks for evaluation and integration of data in regulatory evaluations 5.Harmonization across regulatory agencies 6.Read-across methods and evaluations -Contemporary Reviews on policy related Research issues -Letters to the Editor -Guest Editorials (by Invitation)
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