ISO/DIS 21474-3

In vitro diagnostic medical devices — Multiplex molecular testing for nucleic acids — Part 3: Interpretation and reports ISO/DIS 21474-3

General information

40.99 Full report circulated: DIS approved for registration as FDIS   Mar 1, 2024

ISO

ISO/TC 212 Clinical laboratory testing and in vitro diagnostic test systems

International Standard

11.100.10   In vitro diagnostic test systems

Scope

This document gives general requirements for interpretation and reports of multiplex molecular tests using IVD medical devices and laboratory developed tests (LDTs), including qualitative/quantitative detection of nucleic acid targets.
This document is applicable to all the methods that are used for IVD medical devices and LDTs that measure two or more nucleic acid targets of interest. This document is intended for multiplex assays that evaluate human nucleic acid targets, and detection of microbial pathogens in the background of human genome directly from clinical specimens.

Life cycle

NOW

IN_DEVELOPMENT
ISO/DIS 21474-3
40.99 Full report circulated: DIS approved for registration as FDIS
Mar 1, 2024