Registration number (WIID)Project No.TitleStatus
31365EN ISO 19001:2013In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology (ISO/DIS 19001:2010)Izstrādē
60920prEN ISO 15197 revIn vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitusIzstrādē
67446CEN/TS 17626:2021Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for human specimen - Isolated microbiome DNAIzstrādē
73607FprEN ISO 15193In vitro diagnostic medical devices - Requirements for reference measurement procedures (ISO/FDIS 15193:2026)Izstrādē
68138CEN/TS 17742:2022Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free RNA from plasmaIzstrādē
61693EN ISO 20166-1:2018Molecular in-vitro diagnostic examinations - Specifications for preexamination processes for formalin-fixed and paraffin-embedded (FFPE) tissue - Part 1: Isolated RNA (ISO/DIS 20166-1:2016)Izstrādē
25089prEN ISO 15193In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Presentation of reference measurement proceduresIzstrādē
81455prEN ISO 25379-2In vitro diagnostic Next Generation Sequencing (NGS) workflows -- Part 2: Human RNA examinationIzstrādē
70517EN ISO 20184-3:2021Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for frozen tissue - Part 3: Isolated DNA (ISO/DIS 20184-3:2020)Izstrādē
68137CEN/TS 17747:2022Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for exosomes and other extracellular vesicles in venous whole blood - DNA, RNA and proteinsIzstrādē
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