Registration number (WIID)Project No.TitleStatus
79016EN ISO 15189:2022/A11:2023Medical laboratories - Requirements for quality and competenceStandarts spēkā
27341LVS EN ISO 15193:2009In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for content and presentation of reference measurement procedures (ISO 15193:2009)Standarts spēkā
5110LVS EN ISO 18153:2003In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability for catalytic concentration of enzymes assigned to calibrators and control materialsStandarts spēkā
5106LVS EN 13975:2003Sampling procedures used for acceptance testing of in vitro diagnostic medical devices - Statistical aspectsStandarts spēkā
76942LVS CEN ISO/TS 7552-3:2024Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumour cells (CTCs) in venous whole blood - Part 3: Preparations for analytical CTC staining (ISO/TS 7552-3:2024)Standarts spēkā
76942CEN ISO/TS 7552-3:2024Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumour cells (CTCs) in venous whole blood - Part 3: Preparations for analytical CTC staining (ISO/TS 7552-3:2024)Standarts spēkā
5107LVS EN 13641:2003Elimination or reduction of risk of infection related to in vitro diagnostic reagentsStandarts spēkā
61390LVS EN ISO 15195:2019Laboratory medicine - Requirements for the competence of calibration laboratories using reference measurement procedures (ISO 15195:2018)Standarts spēkā
5109LVS EN 13532:2003General requirements for in vitro diagnostic medical devices for self-testingStandarts spēkā
60817LVS EN ISO 23640:2015In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)Standarts spēkā
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