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定量生物分析方法的验证与实施:色谱及配体结合分析的最佳实践

Quantitative bioanalytical methods validation and implementation: best practices for chromatographic and ligand binding assays.

作者信息

Viswanathan C T, Bansal Surendra, Booth Brian, DeStefano Anthony J, Rose Mark J, Sailstad Jeffrey, Shah Vinod P, Skelly Jerome P, Swann Patrick G, Weiner Russell

机构信息

Food and Drug Administration, Center for Drug Evaluation and Research, Rockville, Maryland 20857, USA.

出版信息

Pharm Res. 2007 Oct;24(10):1962-73. doi: 10.1007/s11095-007-9291-7. Epub 2007 Apr 26.

Abstract

The Third AAPS/FDA Bioanalytical Workshop, entitled "Quantitative Bioanalytical Methods Validation and Implementation: Best Practices for Chromatographic and Ligand Binding Assays" was held on May 1-3, 2006 in Arlington, VA. The format of this workshop consisted of presentations on bioanalytical topics, followed by discussion sessions where these topics could be debated, with the goal of reaching consensus, or identifying subjects where addition input or clarification was required. The discussion also addressed bioanalytical validation requirements of regulatory agencies, with the purpose of clarifying expectations for regulatory submissions. The proceedings from each day were reviewed and summarized in the evening sessions among the speakers and moderators of the day. The consensus summary was presented back to the workshop on the last day and was further debated. This communication represents the distillate of the workshop proceedings and provides the summary of consensus reached and also contains the validation topics where no consensus was reached.

摘要

第三届美国药学科学家协会/美国食品药品监督管理局生物分析研讨会,题为“定量生物分析方法的验证与实施:色谱分析和配体结合分析的最佳实践”,于2006年5月1日至3日在弗吉尼亚州阿灵顿市举行。本次研讨会的形式包括生物分析主题的演讲,随后是讨论环节,在该环节中可以对这些主题进行辩论,目的是达成共识,或确定需要额外投入或澄清的主题。讨论还涉及监管机构的生物分析验证要求,以明确对监管申报的期望。每天的会议记录在当天的发言者和主持人之间的晚间会议中进行了审查和总结。共识总结在最后一天提交给研讨会并进行了进一步辩论。本通讯代表了研讨会会议记录的精华,提供了达成的共识总结,还包含未达成共识的验证主题。

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