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dc.contributor.authorRambla Alegre, María
dc.contributor.authorEsteve-Romero, Josep
dc.contributor.authorCarda-Broch, Samuel
dc.date.accessioned2013-05-27T14:08:14Z
dc.date.available2013-05-27T14:08:14Z
dc.date.issued2012
dc.identifier.citationJournal of Chromatography A Volume 1232, 6 April 2012, Pages 101–109 Selected Papers from the 36th International Symposium on High-Performance Liquid Phase Separations and Related Techniquesca_CA
dc.identifier.issn0021-9673
dc.identifier.issn1873-3778
dc.identifier.urihttp://hdl.handle.net/10234/64753
dc.description.abstractMethod validation is an important requirement in the practice of chemical analysis. However, awareness of its importance, why it should be done and when, and exactly what needs to be done, seems to be poor amongst analytical chemists. Much advice related to method validation already exists in the literature, especially related to particular methods, but more often than not is underused. Some analysts see method validation as something that can only be done by collaborating with other laboratories and therefore do not go about it. In addition, analysts’ understanding of method validation is inhibited by the fact that many of the technical terms used in the processes for evaluating methods vary in different sectors of analytical measurement, both in terms of their meaning and the way they are determined. Validation applies to a defined protocol, for the determination of a specified analyte and range of concentrations in a particular type of test material, used for a specified purpose. In general, validation should check that the method performs adequately for the purpose throughout the range of analyte concentrations and test materials to which it is applied. It follows that these features, together with a statement of any fitness-for-purpose criteria, should be completely specified before any validation takes place.ca_CA
dc.format.extent8 p.ca_CA
dc.format.mimetypeapplication/pdfca_CA
dc.language.isoengca_CA
dc.publisherElsevierca_CA
dc.relation.isPartOfJournal of Chromatography A, 2012, Vol. 1232. Selected Papers from the 36th International Symposium on High-Performance Liquid Phase Separations and Related Techniquesca_CA
dc.rightsCopyright © 2011 Elsevier B.V. All rights reserved.ca_CA
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/*
dc.subjectMethod validationca_CA
dc.subjectAnalytical proceduresca_CA
dc.subjectChemical analysisca_CA
dc.subjectGuidelinesca_CA
dc.subjectRegulatory agenciesca_CA
dc.subjectReliabilityca_CA
dc.titleIs it really necessary to validate an analytical method or not? That is the questionca_CA
dc.typeinfo:eu-repo/semantics/articleca_CA
dc.identifier.doihttp://dx.doi.org/10.1016/j.chroma.2011.10.050
dc.rights.accessRightsinfo:eu-repo/semantics/restrictedAccessca_CA
dc.relation.publisherVersionhttp://www.sciencedirect.com/science/article/pii/S0021967311015743ca_CA
dc.type.versioninfo:eu-repo/semantics/publishedVersionca_CA


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