New advances in method validation and measurement uncertainty aimed at improving the quality of chemical data

被引:155
作者
Feinberg, M
Boulanger, B
Dewé, W
Hubert, P
机构
[1] INRA, F-75231 Paris 05, France
[2] Lilly Dev Ctr, B-1348 Mont St Guibert, Belgium
[3] Univ Liege, CHU, Inst Pharm, Dept Analyt & Pharmaceut Chem, B-4000 Liege, Belgium
关键词
data quality; nethod validation; beta-expectation tolerance interval; uncertainty;
D O I
10.1007/s00216-004-2791-y
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The implementation of quality systems in analytical laboratories has now, in general, been achieved. While this requirement significantly modified the way that the laboratories were run, it has also improved the quality of the results. The key idea is to use analytical procedures which produce results that fulfil the users' needs and actually help when making decisions. This paper presents the implications of quality systems on the conception and development of an analytical procedure. It introduces the concept of the life-cycle of a method as a model that can be used to organize the selection, development, validation and routine application of a method. It underlines the importance of method validation, and presents a recent approach based on the accuracy profile to illustrate how validation must be fully integrated into the basic design of the method. Thanks to the beta-expectation tolerance interval introduced by Mee (Technometrics (1984) 26(3):251-253), it is possible to unambiguously demonstrate the fitness for purpose of a new method. Remembering that it is also a requirement for accredited laboratories to express the measurement uncertainty, the authors show that uncertainty can be easily related to the trueness and precision of the data collected when building the method accuracy profile.
引用
收藏
页码:502 / 514
页数:13
相关论文
共 19 条
[1]  
[Anonymous], MAN GUID VAM VAL AN
[2]  
[Anonymous], 2003, 21748 ISODTS
[3]  
[Anonymous], 1998, FITN PURP AN METH LA
[4]  
[Anonymous], STP PHARM PRATIQUES
[5]  
BOULANGER B, 2000, AAPS C APQ OP FOR IN
[6]  
CHAPUZET E, 1998, STP PHARM PRATIQUES, V8, P81
[7]  
Chapuzet E., 1997, STP Pharma Pratiques, V7, P169
[8]   Development and validation of an automated method for the liquid chromatographic determination of sotalol in plasma using dialysis and trace enrichment on a cation-exchange pre-column as on-line sample preparation [J].
Chiap, P ;
Ceccato, A ;
Buraglia, BM ;
Boulanger, B ;
Hubert, P ;
Crommen, J .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2001, 24 (5-6) :801-814
[9]  
*EURACHEM CIRTAC, 2000, GUID QUANT UNC AN ME
[10]   Comparison of strategies to quantify uncertainty of lead measurements in biological tissue at mg kg-1 level [J].
Feinberg, M ;
Montamat, M ;
Rivier, C ;
Lalère, B ;
Labarraque, G .
ACCREDITATION AND QUALITY ASSURANCE, 2002, 7 (10) :403-408