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Ante la necesidad crítica de conocer la fiabilidad y efectividad de los resultados expresados por los Kits diagnóstico inmunocromatografia de flujo lateral, Leitat ha puesto en marcha un proceso para la validación de proveedores de estos “KITS” tanto en muestras de sangre como en plasma. La validación de “KITS” se realiza por método propio cuyo diseño ha incluido un pequeño ensayo clínico. El método nos permite entender la utilidad del “KIT” en diferentes momentos temporales de la enfermedad, su eficacia VS la técnica de RT-PCR y la eficacia entre usar el mismo kit en sangre VS plasma.
Equipo de diagnóstico fotónico por la cuantificación de RNA vírico sin amplificación por PCR, por los departamentos de Energía e Ingeniería.
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