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Safety pharmacology methods and models in an evolving regulatory environment

机译:在不断变化的监管环境中的安全药理学方法和模型

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This editorial prefaces the annual themed issue on safety pharmacology (SP) methods published in the Journal of Pharmacological and Toxicological Methods (JPTM). We highlight here the content derived from the recent 2016 Safety Pharmacology Society (SPS), Canadian Society of Pharmacology and Therapeutics (CSPT), and Japanese Safety Pharmacology Society (JSPS) joint meeting held in Vancouver, B.C., Canada. This issue of JPTM continues the tradition of providing a publication summary of articles primarily presented at the joint meeting with direct bearing on the discipline of SP. As the regulatory landscape is expected to evolve with revision announced for the existing guidance document on non-clinical proarrhythmia risk assessment (ICHS7B) there is also imminent inception of the Comprehensive in vitro Proarrhythmia Assay (CiPA) initiative. Thus, the field of SP is dynamically progressing with characterization and implementation of numerous alternative non-clinical safety models. Novel method development and refinement in all areas of the discipline are reflected in the content.
机译:这次编辑旨在在药理和毒理学方法(JPTM)杂志上公布的安全药物学(SP)方法的年度主题问题。我们突出了来自2016年最近的2016年安全药理学协会(SPS),加拿大药理和治疗学会(CSPT)和日本安全药理学协会(JSP)联席会议,加拿大加拿大加拿大加拿大。这一问题JPTM仍在继续提供主要介绍的文章摘要的传统,主要在联合会议上与SP的纪律直接承担。由于监管景观预计随着关​​于非临床前期风险评估的现有指导文件(ICHS7B)宣布的修订版,还迫切地初始化了全面的体外预血淋淋性测定(CIPA)倡议。因此,SP的领域是用许多替代的非临床安全模型的表征和实现动态进展。纪律的所有领域的新型方法开发和改进反映在内容中。

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