This document specifies requirements and gives recommendations for the handling, documentation and processing of urine, venous blood plasma and serum intended for metabolomics analysis in the pre-examination processes. This document is applicable to metabolomics examinations and can be used by biomedical laboratories, customers of laboratories, in vitro diagnostics developers and manufacturers, institutions and companies performing biomedical research, biobanks, and regulatory authorities.
Status: PublishedPublication date: 2021-05
Edition: 1Number of pages: 18
Technical Committee: ISO/TC 212 Clinical laboratory testing and in vitro diagnostic test systems
- ICS :
- 11.100.10 In vitro diagnostic test systems
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|std 1 92||PDF + ePub|
|std 2 92||Paper|
ISO 23118:2021Stage: 60.60
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