DIN CEN/TS 16945*DIN SPEC 13228:2016-11

This Technical Specification gives recommendations for the handling, documentation and processing of urine, plasma and serum generated from whole blood intended for metabolomics analysis during the pre-analytical phase before metabolomic profiling is performed. This Technical Specification is applicable to molecular diagnostic examinations (e. g. in-vitro diagnostic laboratories, laboratory customers, in-vitro diagnostics developers and manufacturers, institutions and companies performing biomedical research, biobanks, and regulation authorities). The concentration of some metabolites can undergo significant changes after collection, as an answer to different operating procedures. Special measures have to be taken to secure good quality of urine, serum and plasma samples for the metabolomics analysis of this biofluids.