Resumen
This document describes the particular clinical laboratory practice requirements to ensure the quality of detection, identification and quantification of microbial pathogens using nucleic acid amplification tests (NAAT).
It is intended for use by laboratories that develop, and/or implement and use, or perform NAAT for medical, research or health-related purposes. This document does not apply to the development of in vitro diagnostic (IVD) medical devices by manufacturers. However, it does include verification and validation of such devices and/or the corresponding processes when implemented and used by the laboratories.
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Informaciones generales
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Estado: PublicadoFecha de publicación: 2020-11
Versión corregida (en): 2020-12Etapa: Norma Internacional publicada [60.60] -
Edición: 1Número de páginas: 39
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Comité Técnico :ISO/TC 212ICS :11.100.01
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Ciclo de vida
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Anteriormente
RetiradaISO/TS 17822-1:2014
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Ahora
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