Key elements of bioanalytical method validation for small molecules

被引:266
作者
Bansal, Surendra
DeStefano, Anthony
机构
[1] Hoffmann La Roche Inc, Nutley, NJ 07110 USA
[2] Procter & Gamble Pharmaceut, Mason, OH USA
关键词
bioanalytical; validation; precision; accuracy; sensitivity; selectivity; reproducibility;
D O I
10.1208/aapsj0901011
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Method validation is a process that demonstrates that a method will successfully meet or exceed the minimum standards recommended in the Food and Drug Administration (FDA) guidance for accuracy, precision, selectivity, sensitivity, reproducibility, and stability. This article discusses the validation of bioanalytical methods for small molecules with emphasis on chromatographic techniques. We present current thinking on validation requirements as described in the current FDA Guidance and subsequent 2006 Bioanalytical Methods Validation Workshop white paper.
引用
收藏
页码:E109 / E114
页数:6
相关论文
共 2 条
[1]  
Food and Drug Administration, 2001, FDA GUID IND BIOAN M
[2]   Workshop/conference report - Quantitative bioanalytical methods validation and implementation: Best practices for chromatographic and ligand binding assays [J].
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 .
AAPS JOURNAL, 2007, 9 (01) :E30-E42