{"id":46,"date":"2025-11-13T22:16:26","date_gmt":"2025-11-13T22:16:26","guid":{"rendered":"https:\/\/www.research.colostate.edu\/integrity-security-compliance\/quality-assurance\/method-validation\/"},"modified":"2025-11-13T22:37:10","modified_gmt":"2025-11-13T22:37:10","slug":"method-validation","status":"publish","type":"page","link":"https:\/\/www.research.colostate.edu\/integrity-security-compliance\/quality-assurance\/qa-services\/method-validation\/","title":{"rendered":"Method Validation"},"content":{"rendered":"\n<p>The objective of method validation is to <strong>demonstrate that procedures you use are suitable for their intended purpose.<\/strong> Selective and sensitive methods for the quantitative evaluation of drugs and their metabolites are critical for the successful conduct of preclinical and\/or biopharmaceutics and clinical pharmacology studies; therefore, having confidence in method results are essential in safety research as well as many other research outlets. Method validation includes systematically assessing the procedures to demonstrate that a particular method used for quantitative measurement of analytes in a given biological matrix, such as blood, plasma, serum, or urine, is reliable and reproducible for the intended use.<\/p>\n\n\n\n<div class=\"wp-block-group is-layout-constrained wp-block-group-is-layout-constrained\" style=\"margin-bottom:3rem\">\n<ul class=\"wp-block-list is-style-green-border\">\n<li>The fundamental parameters for this validation include: (1) accuracy, (2) precision, (3) selectivity, (4) sensitivity, (5) reproducibility, and (6) stability. Validation involves planning and documenting, through specific laboratory investigations, that the method&#8217;s performance characteristics are suitable and reliable for the intended applications. The acceptability of the data corresponds directly to the criteria used to validate the method.<\/li>\n<\/ul>\n<\/div>\n\n\n\n<div class=\"wp-block-columns is-layout-flex wp-container-core-columns-is-layout-28f84493 wp-block-columns-is-layout-flex\">\n<div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\">\n<h2 class=\"wp-block-heading\">US Regulatory References \/ Guidances<\/h2>\n\n\n\n<ul class=\"wp-block-list\">\n<li><strong><a href=\"http:\/\/www.fda.gov\/downloads\/Drugs\/GuidanceComplianceRegulatoryInformation\/Guidances\/UCM070107.pdf\" target=\"_blank\" rel=\"noreferrer noopener\">FDA Guidance for Industry for Bioanalytical Method Validation<\/a><\/strong><\/li>\n\n\n\n<li><strong><a href=\"https:\/\/www.fda.gov\/media\/87801\/download\" target=\"_blank\" rel=\"noreferrer noopener\">&nbsp;FDA Guidance for Industry for Analytical Procedures and Methods Validation for Drugs and Biologics<\/a><\/strong><\/li>\n<\/ul>\n<\/div>\n\n\n\n<div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\">\n<h2 class=\"wp-block-heading\">International References \/ Guidances<\/h2>\n\n\n\n<ul class=\"wp-block-list\">\n<li><a href=\"https:\/\/www.ich.org\/fileadmin\/Public_Web_Site\/ICH_Products\/Guidelines\/Quality\/Q2_R1\/Step4\/Q2_R1__Guideline.pdf\" target=\"_blank\" rel=\"noreferrer noopener\"><strong>ICH ICH Harmonised Tripartite Guideline for Validation of Analytical Procedures: Text and Methodology Q2(R1)<\/strong><\/a><\/li>\n\n\n\n<li><a href=\"http:\/\/www.ema.europa.eu\/docs\/en_GB\/document_library\/Scientific_guideline\/2011\/08\/WC500109686.pdf\" target=\"_blank\" rel=\"noreferrer noopener\"><strong>&nbsp;EMA European Medicines Agency (EMA) Guideline on Bioanalytical Method Validation<\/strong><\/a><\/li>\n\n\n\n<li><strong><a href=\"http:\/\/www.ema.europa.eu\/docs\/en_GB\/document_library\/Scientific_guideline\/2009\/09\/WC500002662.pdf\" target=\"_blank\" rel=\"noreferrer noopener\">&nbsp;EMA European Medicines Agency Guideline on Analytical Method Validation<\/a><\/strong><\/li>\n\n\n\n<li><strong><a href=\"http:\/\/www.globalbioanalysisconsortium.org\/\" target=\"_blank\" rel=\"noreferrer noopener\">GBC Global Bioanalysis Consortium<\/a><\/strong><\/li>\n<\/ul>\n<\/div>\n<\/div>\n\n\n\n<p><\/p>\n","protected":false},"excerpt":{"rendered":"<p>The objective of method validation is to demonstrate that procedures you use are suitable for their intended purpose. Selective and sensitive methods for the quantitative evaluation of drugs and their metabolites are critical for the successful conduct of preclinical and\/or biopharmaceutics and clinical pharmacology studies; therefore, having confidence in method results are essential in safety [&hellip;]<\/p>\n","protected":false},"author":6,"featured_media":0,"parent":38,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"microsite":[6],"class_list":["post-46","page","type-page","status-publish","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/www.research.colostate.edu\/integrity-security-compliance\/wp-json\/wp\/v2\/pages\/46","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.research.colostate.edu\/integrity-security-compliance\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.research.colostate.edu\/integrity-security-compliance\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.research.colostate.edu\/integrity-security-compliance\/wp-json\/wp\/v2\/users\/6"}],"replies":[{"embeddable":true,"href":"https:\/\/www.research.colostate.edu\/integrity-security-compliance\/wp-json\/wp\/v2\/comments?post=46"}],"version-history":[{"count":0,"href":"https:\/\/www.research.colostate.edu\/integrity-security-compliance\/wp-json\/wp\/v2\/pages\/46\/revisions"}],"up":[{"embeddable":true,"href":"https:\/\/www.research.colostate.edu\/integrity-security-compliance\/wp-json\/wp\/v2\/pages\/38"}],"wp:attachment":[{"href":"https:\/\/www.research.colostate.edu\/integrity-security-compliance\/wp-json\/wp\/v2\/media?parent=46"}],"wp:term":[{"taxonomy":"microsite","embeddable":true,"href":"https:\/\/www.research.colostate.edu\/integrity-security-compliance\/wp-json\/wp\/v2\/microsite?post=46"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}