Registration number (WIID)Project No.TitleStatus
27618EN ISO 18113-3:2009In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO/FDIS 18113-3:2009)Atcelts
65451CEN/TS 17390-3:2020Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood - Part 3: Preparations for analytical CTC stainingAtcelts
41033CEN/TS 16826-1:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for snap frozen tissue - Part 1: Isolated RNAAtcelts
64590CEN/TS 16826-3:2018Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for snap frozen tissue - Part 3: Isolated DNAAtcelts
37593EN ISO 18113-5:2011In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009)Atcelts
67448CEN/TS 17688-3:2021Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for Fine Needle Aspirates (FNAs) - Part 3: Isolated genomic DNAAtcelts
67447CEN/TS 17688-1:2021Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for Fine Needle Aspirates (FNAs) - Part 1: Isolated cellular RNAAtcelts
33817EN ISO 15197:2013In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO/DIS 15197:2011)Atcelts
29669EN ISO 15189:2012Medical laboratories - Requirements for quality and competence (ISO/DIS 15189:2011)Atcelts
81455prEN ISO 25379-2In vitro diagnostic Next Generation Sequencing (NGS) workflows -- Part 2: Human RNA examinationIzstrādē
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