Aplicación de metas analíticas y modelo Seis Sigma en la evaluación del control de calidad de Química Clínica

Based on our results we can suggest that an adequate quality control model in Clinical Chemistry could initially include the establishment of analytical specifications based on CLIA for those analytes with low biological variation, and the desirable goals of biological variation for the rest of the analytes. Both goals can be achieved by the instruments used in this study.