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.
État actuel: PubliéeDate de publication: 2020-11
Version corrigée (en): 2020-12
Comité technique: ISO/TC 212 Laboratoires de biologie médicale et systèmes de diagnostic in vitro
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|std 1 166||PDF + ePub|
|std 2 166||Papier|