90.60 Close of review Sep 3, 2026
ISO
ISO/TC 212 Clinical laboratory testing and in vitro diagnostic test systems
International Standard
11.100.10 In vitro diagnostic test systems
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.
PUBLISHED
ISO 23118:2021
90.60
Close of review
Sep 3, 2026