Regulatory Toxicology and Pharmacology

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)

《监管毒理学和药理学》是一本国际学术期刊，刊登同行评议文章，内容涉及动物和人体实验数据的生成、评估和解释，这些数据对监管机构制定社会毒理学和药理学法规具有直接的重要性和相关性。所有发表的同行评审文章都应致力于改善对人类健康和环境的保护。欢迎在科学基础上对毒理学和药理学化合物的风险评估和管理方面的法律和/或监管决策进行评论和讨论。它面向国际读者群，包括科学家、风险评估员和管理人员，以及活跃在人类和环境健康领域的其他专业人士。