Harmonization of strategies for the validation of quantitative analytical procedures - A SFSTP proposal - Part III

被引:291
作者
Hubert, Ph.
Nguyen-Huu, J.-J.
Boulangerc, B.
Chapuzet, E.
Cohen, N.
Compagnon, P.-A.
Dewe, W.
Feinberg, M.
Laurentie, M.
Mercier, N.
Muzard, G.
Valat, L.
Rozet, E.
机构
[1] Univ Liege, CHU, Inst Pharm, Bioanalyt Chem Res Unit,Lab Analyt Chem, B-4000 Liege, Belgium
[2] Sanofi Aventis, Quai Jules Guesde, F-94403 Vitry Sur Seine, France
[3] UCB Pharma SA, Chemin Foriest, B-1420 Braine Lalleud, Belgium
[4] Qualilab, F-45160 Olivet, Orleans, France
[5] Expanscience, F-28231 Epernon, France
[6] French Agcy Hlth Prod Safety AFSSAPS, F-93285 St Denis, France
[7] GlaxoSmithKline Biol, B-1330 Rixensart, Belgium
[8] INRA, Met Risk, F-75231 Paris, France
[9] French Food Safety Agcy AFSSA, LERMDV, F-35032 Fougeres, France
[10] Merck Theramex, F-98007 Monaco, Monaco
[11] Viatris Mfg, F-33701 Merignac, France
关键词
analytical validation; statistics; total error; risk; accuracy profile;
D O I
10.1016/j.jpba.2007.06.032
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In the first two documents [Ph. Hubert, J.J. Nguyen-Huu, B. Boulanger, E. Chapuzet, P. Chiap, N. Cohen, P.A. Compagnon, W. Dewe, M. Feinberg. M. Lallier, M. Laurentie, N. Mercier, G. Muzard, C. Nivet, L. Valat, J. Pharm. Biomed. Anal. 36 (2004) 579-586; Ph. Hubert, J.J. Nguyen-Huu. B. Boulanger, E. Chapuzet, P. Chiap, N. Cohen, P.A. Compagnon, W. Dewe, M. Feinberg, M. Lallier, M. Laurentie, N. Mercier, G. Muzard. C. Nivet, L. Valat, E. Rozet, J. Pharm. Biomed. Anal., in press], a recent SFSTP Commission on the validation of analytical procedure has introduced a harmonized approach for the validation of analytical procedures. In order to complete this guide, the statistical methodology allowing to correctly conclude about the validity of a procedure is proposed in this third part of the guide. Indeed all the steps to obtain the decision tool namely the accuracy profile are described and illustrated step by step by a numerical example. This tool, based on the concept of total error (bias + standard deviation) build with a P-expectation tolerance interval, allows to easily take the right decision and simultaneously minimizing the risk of the future use of the analytical procedure. (C) 2007 Elsevier B.V. All rights reserved.
引用
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页码:82 / 96
页数:15
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*USDA FDA CDER CBE, 2000, GUID IND AN PROC MET