药物开发
免疫分析
生物标志物
计算机科学
适应(眼睛)
风险分析(工程)
质量(理念)
药品
数据科学
生化工程
医学
药理学
工程类
化学
生物
认识论
哲学
抗体
神经科学
免疫学
生物化学
作者
Masood U Khan,Ronald R. Bowsher,Mark J. Cameron,Viswanath Devanarayan,Steve Keller,Lindsay King,Jean Lee,Alyssa Morimoto,Paul Rhyne,Laurie Stephen,Yuling Wu,Timothy Wyant,D. Richard Lachno
出处
期刊:Bioanalysis
[Newlands Press Ltd]
日期:2015-01-01
卷期号:7 (2): 229-242
被引量:39
摘要
Increasingly, commercial immunoassay kits are used to support drug discovery and development. Longitudinally consistent kit performance is crucial, but the degree to which kits and reagents are characterized by manufacturers is not standardized, nor are the approaches by users to adapt them and evaluate their performance through validation prior to use. These factors can negatively impact data quality. This paper offers a systematic approach to assessment, method adaptation and validation of commercial immunoassay kits for quantification of biomarkers in drug development, expanding upon previous publications and guidance. These recommendations aim to standardize and harmonize user practices, contributing to reliable biomarker data from commercial immunoassays, thus, enabling properly informed decisions during drug development.
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