Registration number (WIID)Project No.TitleStatus
61686LVS EN ISO 20186-3:2020Molecular in-vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 3: Isolated circulating cell free DNA from plasma (ISO 20186-3:2019)Standarts spēkā
61695LVS EN ISO 20184-2:2019Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for frozen tissue - Part 2: Isolated proteins (ISO 20184-2:2018)Standarts spēkā
65452LVS CEN/TS 17390-2:2020Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood - Part 2: Isolated DNAStandarts spēkā
70517LVS EN ISO 20184-3:2021Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for frozen tissue - Part 3: Isolated DNA (ISO 20184-3:2021)Standarts spēkā
68065LVS EN ISO 23162:2021Basic semen examination - Specification and test methods (ISO 23162:2021)Standarts 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
70932EN ISO 18113-4:2024In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2022)Standarts spēkā
68157EN ISO 15189:2022Medical laboratories - Requirements for quality and competence (ISO 15189:2022)Standarts spēkā
62263EN 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
61692LVS EN ISO 6710:2017Single-use containers for human venous blood specimen collection (ISO 6710:2017)Standarts spēkā
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