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国际协调会议;动物慢性毒性试验持续时间指南(啮齿类和非啮齿类毒性试验);可获取性。通知。美国卫生与公众服务部食品药品管理局

International Conference on Harmonisation; guidance on the duration of chronic toxicity testing in animals (rodent and nonrodent toxicity testing); availability. Notice. Food and Drug Administration, HHS.

出版信息

Fed Regist. 1999 Jun 25;64(122):34259-60.

Abstract

The Food and Drug Administration (FDA) is publishing a guidance entitled "S4A Duration of Chronic Toxicity Testing in Animals (Rodent and Nonrodent Toxicity Testing)." The guidance was prepared under the auspices of the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) and is intended to provide guidance on the duration of chronic toxicity testing in rodents and nonrodents as part of the safety evaluation of a drug product. FDA is also noting circumstances in which it may accept durations of chronic toxicity testing in nonrodents that differ from the duration generally recommended by ICH.

摘要

美国食品药品监督管理局(FDA)正在发布一份题为《S4A 动物慢性毒性试验的持续时间(啮齿动物和非啮齿动物毒性试验)》的指南。该指南是在人用药品注册技术要求国际协调会议(ICH)的主持下制定的,旨在为作为药品安全性评估一部分的啮齿动物和非啮齿动物慢性毒性试验的持续时间提供指导。FDA 还指出了可能接受与 ICH 一般推荐持续时间不同的非啮齿动物慢性毒性试验持续时间的情况。

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