CLSI ISO 17822:2020
In vitro diagnostic test systems — Nucleic acid amplification-based examination procedures for detection and identification of microbial pathogens - Laboratory quality practice guide
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.
This document is available in electronic format only.
Details
Date of Publication: November 1, 2020
Order Code PDF: CLSI ISO17822E
Order Code Print: print not available
Edition: First
Pages: 39
CLSI ISO 17822:2020 Additional Details
Technical Committee : ISO/TC 212 Clinical laboratory testing and in vitro diagnostic test systems.
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