Critical analysis of several analytical method validation strategies in the framework of the fit for purpose concept

被引:50
作者
Bouabidi, A. [2 ]
Rozet, E. [1 ]
Fillet, M. [3 ]
Ziemons, E. [1 ]
Chapuzet, E. [4 ]
Mertens, B. [5 ]
Klinkenberg, R. [5 ]
Ceccato, A. [6 ]
Talbi, M. [2 ]
Streel, B. [5 ]
Bouklouze, A. [7 ]
Boulanger, B. [8 ]
Hubert, Ph. [1 ]
机构
[1] Univ Liege, Inst Pharm, Analyt Chem Lab, CHU,CIRM, B-4000 Liege, Belgium
[2] Univ Hassan II Mohammedia, UFR Sci & Procedes Anal Physicochim, Analyt Chem Lab, Fac Sci Ben MSik, Casablanca, Morocco
[3] Univ Liege, Inst Pharm, Analyt Pharmaceut Chem Lab, CIRM, B-4000 Liege, Belgium
[4] Qualilab, F-45160 Olivet, France
[5] Galephar MF, B-6900 Marche En Famenne, Belgium
[6] Mithra Pharmaceut SA, B-4000 Liege, Belgium
[7] Univ Med V Soussi, Fac Med & Pharm, Lab Pharmacol Toxicol, Rabat, Morocco
[8] UCB Pharma SA, B-1420 Braine Lalleud, Belgium
关键词
Validation methodology; Accuracy profile; Tolerance intervals; Hypothesis tests; Total error; Fit for purpose; QUANTITATIVE ANALYTICAL PROCEDURES; SFSTP PROPOSAL; CHROMATOGRAPHIC METHODS; WASHINGTON CONFERENCE; TOLERANCE INTERVALS; PART I; HARMONIZATION; GUIDE; ERROR;
D O I
10.1016/j.chroma.2009.08.051
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Analytical method validation is a mandatory step at the end of the development in all analytical laboratories. It is a highly regulated step of the life cycle of a quantitative analytical method. However, even if some documents have been published there is a lack of clear guidance for the methodology to follow to adequately decide when a method can be considered as valid. This situation has led to the availability of several methodological approaches and it is therefore the responsibility of the analyst to choose the best one. The classical decision processes encountered during method validation evaluation are compared, namely the descriptive, difference and equivalence approaches. Furthermore a validation approach using accuracy profile computed by means of beta-expectation tolerance interval and total measurement error is also available. In the present paper all of these different validation approaches were applied to the validation of two analytical methods. The evaluation of the producer and consumer risks by Monte Carlo simulations were also made in order to compare the appropriateness of these various approaches. The classical methodologies give rise to inadequate and contradictory conclusions which do not allow them to answer adequately the objective of method validation, i.e. to give enough guarantees that each of the future results that will be generated by the method during routine use will be close enough to the true value. It is found that the validation methodology which gives the most guarantees with regards to the reliability or adequacy of the decision to consider a method as valid is the one based on the use of the accuracy profile. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:3180 / 3192
页数:13
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