{"id":6153,"date":"2018-04-06T16:52:19","date_gmt":"2018-04-06T14:52:19","guid":{"rendered":"http:\/\/www.phytocontrol.com\/?p=6153"},"modified":"2018-04-16T16:53:18","modified_gmt":"2018-04-16T14:53:18","slug":"criterios-de-validacion-de-un-metodo-de-analisis","status":"publish","type":"post","link":"https:\/\/stagingphytocontrol.shdesign.fr\/es\/noticias\/criterios-de-validacion-de-un-metodo-de-analisis\/","title":{"rendered":"Criterios de validaci\u00f3n de un m\u00e9todo de an\u00e1lisis"},"content":{"rendered":"<p>La validaci\u00f3n de un m\u00e9todo de an\u00e1lisis permite garantizar que el resultado obtenido sea lo m\u00e1s cercano posible al valor de referencia real de una muestra.<\/p>\n<p>&nbsp;<\/p>\n<p>Varios normas, gu\u00edas t\u00e9cnicas y reglamentos establecen requisitos con respecto a las t\u00e9cnicas y los criterios de rendimiento de un m\u00e9todo de an\u00e1lisis<\/p>\n<p>En particular la norma NFT 90-210, la norma NF V03-110, los LAB GTA redactados por COFRAC y el Documento SANTE\/11813\/2017 para los residuos de pesticidas.<\/p>\n<p>&nbsp;<\/p>\n<p>Los criterios que deben validarse son:<\/p>\n<p>&#8211; <strong><u>LD:<\/u><\/strong> L\u00edmite de Detecci\u00f3n,\u00a0corresponde a la concentraci\u00f3n m\u00e1s peque\u00f1a de la sustancia que se puede detectar, pero no cuantificar, en las condiciones experimentales descritas en el m\u00e9todo.<\/p>\n<p>Dicho de otra manera, es el l\u00edmite por debajo del cual el analito se considera &#8220;no detectado&#8221;.<\/p>\n<p>&nbsp;<\/p>\n<p>&#8211; <strong><u>LQ:<\/u><\/strong> Limitaci\u00f3n de Cuantificaci\u00f3n,\u00a0es la concentraci\u00f3n m\u00e1s peque\u00f1a de la sustancia que puede ser cuantificada con una incertidumbre aceptable en las condiciones experimentales descritas del m\u00e9todo.<\/p>\n<p>&nbsp;<\/p>\n<p>&#8211; <strong><u>Precision<\/u><\/strong>: La precision expresa la diferencia entre el valor promedio obtenido a partir de una gran serie de resultados de ensayos y un valor de referencia.<\/p>\n<p>Se determina en relaci\u00f3n con un material de referencia certificado (MRC). En ausencia de MRC, se puede usar un valor que se acepte como un valor convencionalmente verdadero.<\/p>\n<p>&nbsp;<\/p>\n<p>&#8211; <strong><u>Fidelidad<\/u><\/strong><strong><u>:<\/u><\/strong> La fidelidad expresa la estrecha concordancia entre varios resultados del ensayo de una misma muestra homog\u00e9nea en las condiciones prescritas.<\/p>\n<p>&nbsp;<\/p>\n<p>&#8211; condiciones de repetibilidad: condiciones donde los resultados de ensayo independientes se obtienen por el mismo m\u00e9todo sobre individuos de ensayo id\u00e9nticos, en el mismo laboratorio, por el mismo operador, utilizando el mismo equipo y durante un corto intervalo de tiempo.<\/p>\n<p>&nbsp;<\/p>\n<p>&#8211; condiciones de reproductibilidad: condiciones donde los resultados del ensayo se obtienen por el mismo m\u00e9todo en individuos de ensayo id\u00e9nticos en diferentes laboratorios, con diferentes operadores y utilizando equipos diferentes.<\/p>\n<p>&nbsp;<\/p>\n<p>&#8211; <strong><u>Linealidad:<\/u><\/strong> capacidad del m\u00e9todo analitico, dentro de un intervalo, de obtener una respuesta instrumental o resultados proporcionales de la ocncentracion de analito en la muestra por el laboratorio.<\/p>\n<p>&nbsp;<\/p>\n<p>&#8211; <strong><u>Especificidad:<\/u><\/strong> Un procedimiento de analisis se dice que es \u00ab\u00a0especifico\u00a0\u00bb cuando permite garantizar que la se\u00f1al medida proviene solo del analito. Esto es para demostrar que la(s) sustancia(s) cuantificada(s) dentro de la matriz son el(los) analito(s) buscado(s).<\/p>\n<p>&nbsp;<\/p>\n<p>&#8211; <strong><u>Incertidumbre:<\/u><\/strong> parametro asociado al resultado de medicion que caracteriza la dispersion de los valores que razonablemente podrian ser asignados al mesurado.<\/p>\n<p>&nbsp;<\/p>\n<p>&#8211; <strong><u>Robustez:<\/u><\/strong> cualidad de un m\u00e9todo capaz de ofrecer resultados de una exactitud y de una precision aceptables dentro de condiciones diversas.<\/p>\n<p>&nbsp;<\/p>\n<p>La validaci\u00f3n de los m\u00e9todos anal\u00edticos es una etapa clave y fundamental del proceso de acreditaci\u00f3n.<\/p>\n<p>La norma NF EN ISO 17025 exige al laboratorio la validacion de los m\u00e9todos no normalizados, de los m\u00e9todos desarrollados por el laboratorio y los m\u00e9todos normalizados empleados fuera del dominio de aplicacion previsto, o modificados.<\/p>\n<p>&nbsp;<\/p>\n<p>Para cualquier informaci\u00f3n t\u00e9cnica o reglamentaria adicional no dude en contactarnos.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>La validaci\u00f3n de un m\u00e9todo de an\u00e1lisis permite garantizar que el resultado obtenido sea lo&hellip;<\/p>\n","protected":false},"author":2,"featured_media":5902,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[192],"tags":[],"class_list":["post-6153","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-noticias"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.3 - 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