化学药物临床动力学研究指导原则.docVIP

下载本文档

14
0
约1.64万字
约 24页
2016-06-14 发布于重庆
举报
版权申诉

化学药物临床动力学研究指导原则.doc

1、本文档共24页，可阅读全部内容。
2、原创力文档（book118）网站文档一经付费（服务费），不意味着购买了该文档的版权，仅供个人/单位学习、研究之用，不得用于商业用途，未经授权，严禁复制、发行、汇编、翻译或者网络传播等，侵权必究。
3、本站所有内容均由合作方或网友上传，本站不对文档的完整性、权威性及其观点立场正确性做任何保证或承诺！文档内容仅供研究参考，付费前请自行鉴别。如您付费，意味着您自己接受本站规则且自行承担风险，本站不退款、不进行额外附加服务；查看《如何避免下载的几个坑》。如果您已付费下载过本站文档，您可以点击这里二次下载。
4、如文档侵犯商业秘密、侵犯著作权、侵犯人身权等，请点击“版权申诉”（推荐），也可以打举报电话：400-050-0827(电话支持时间：9:00-18:30)。
5、该文档为VIP文档，如果想要下载，成为VIP会员后，下载免费。
6、成为VIP后，下载本文档将扣除1次下载权益。下载后，不支持退款、换文档。如有疑问请联系我们。
7、成为VIP后，您将拥有八大权益，权益包括：VIP文档下载权益、阅读免打扰、文档格式转换、高级专利检索、专属身份标志、高级客服、多端互通、版权登记。
8、VIP文档为合作方或网友上传，每下载1次，网站将根据用户上传文档的质量评分、类型等，对文档贡献者给予高额补贴、流量扶持。如果你也想贡献VIP文档。上传文档

化学药物临床动力学研究指导原则

指导原则编号：【H 】 G CL1-2 化学药物临床药代动力学研究技术指导原则二○○五年三月目录一、概述····················································································································································1 二、药代动力学研究生物样品分析方法的建立和确证···············································2 （一）常用分析方法·················································································································2 （二）方法学确证······················································································································2 1、特异性······································································································································3 2、标准曲线和定量范围······································································································3 3、定量下限·································································································································4 4、精密度与准确度·················································································································4 5、样品稳定性···························································································································5 6、提取回收率··························································································································5 7、微生物学和免疫学分析·······························································································5 8、方法学质控··························································································································6 （三）分析数据的记录与保存··························································································6 1、方法建立与确认的数据·······························································································7 2、样品分析的数据···············································································································7 3、其他相关信息···································································································