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Product | ISO 21474-2:2022 | ||
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Price | Price USD 106.00 | ||
Rating | Rating | ||
Buy | Buy Add to Cart | ||
Description |
Description
This document gives the general requirements for validation and verification of multiplex molecular tests which simultaneously identify two or more nucleic acid target sequences of interest. This document is applicable to all multiplex methods used for examination using IVD medical devices and laboratory developed tests (LDTs). It provides information for both qualitative and quantitative detection of nucleic acid target sequences. This document is intended as guidance for multiplex examinations that either detect and/or quantify human nucleic acid target sequences or microbial pathogen nucleic acid target sequences from human clinical specimens. This document is applicable to any molecular in vitro diagnostic (IVD) examination performed by medical laboratories. It is also intended to be used by laboratory customers, IVD developers and manufacturers, biobanks, institutions, and commercial organizations performing biomedical research and regulatory authorities. This document is not applicable to metagenomics. NOTE An examination procedure developed for a laboratory’s own use is often referred to as a “laboratory developed test,” “LDT,” or “in-house test”. |
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Standard Number | Standard Number ISO 21474-2:2022 | ||
Title | Title ISO 21474-2:2022 In vitro diagnostic medical devices — Multiplex molecular testing for nucleic acids — Part 2: Validation and verification | ||
Status | Status Published | ||
Publication Date | Publication Date 13 May 2022 | ||
Cross References | Cross References | ||
Descriptors | Descriptors | ||
ICS | ICS 11.100.10 | ||
Committee | Committee ISO/TC 212 Clinical laboratory testing and in vitro diagnostic test systems | ||
ISBN | ISBN | ||
Publisher | Publisher PECB Store | ||
Format | Format PDF | ||
Delivery | Delivery NO | ||
Pages | Pages 15 | ||
File Size | File Size KB |