Registration number (WIID)Project No.TitleStatus
79016EN ISO 15189:2022/A11:2023Medical laboratories - Requirements for quality and competenceStandarts spēkā
68066LVS EN ISO 23118:2021Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma (ISO 23118:2021)Standarts spēkā
5109LVS EN 13532:2003General requirements for in vitro diagnostic medical devices for self-testingStandarts spēkā
62263LVS EN ISO 17511:2021In vitro diagnostic medical devices - Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples (ISO 17511:2020)Standarts spēkā
70354LVS EN ISO 16256:2022Clinical laboratory testing and in vitro diagnostic test systems - Broth micro-dilution reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infectious diseases (ISO 16256:2021)Standarts spēkā
72259LVS EN ISO 4307:2022Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for saliva - Isolated human DNA (ISO 4307:2021)Standarts spēkā
5106LVS EN 13975:2003Sampling procedures used for acceptance testing of in vitro diagnostic medical devices - Statistical aspectsStandarts spēkā
68789LVS EN ISO 20166-4:2021Molecular in vitro diagnostic examinations - Specifications for preexamination processes for formalin-fixed and paraffin-embedded (FFPE) tissue - Part 4: In situ detection techniques (ISO 20166-4:2021)Standarts spēkā
67447LVS CEN/TS 17688-1:2022Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for Fine Needle Aspirates (FNAs) - Part 1: Isolated cellular RNAStandarts spēkā
67464LVS CEN/TS 17811:2022Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for urine and other body fluids - Isolated cell free DNAStandarts spēkā
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