Registration number (WIID)Project No.TitleStatus
79016EN ISO 15189:2022/A11:2023Medical laboratories - Requirements for quality and competenceStandarts spēkā
5116LVS EN 12322:2001In vitro diagnostic medical devices - Culture media for microbiology - Performance criteria for culture mediaStandarts spēkā
67445LVS CEN/TS 17688-2:2022Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for Fine Needle Aspirates (FNAs) - Part 2: Isolated proteinsStandarts spēkā
61390LVS EN ISO 15195:2019Laboratory medicine - Requirements for the competence of calibration laboratories using reference measurement procedures (ISO 15195:2018)Standarts spēkā
61863LVS EN ISO 20776-1:2020Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices - Part 1: Broth micro-dilution reference method for testing the in vitro activity of antimicrobial agents against rapidly growing aerobic bacteria involved in infectious diseases (ISO 20776-1:2019, including Corrected version 2019-12)Standarts 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
22397LVS EN 13612:2003 /AC:2003Performance evaluation of in vitro diagnostic medical devicesStandarts spēkā
5111LVS EN 14136:2004Use of external quality assessment schemes in the assessment of the performance of in vitro diagnostic examination proceduresStandarts spēkā
74138LVS CEN/TS 17981-1:2023In vitro diagnostic Next Generation Sequencing (NGS) workflows - Part 1: Human DNA examinationStandarts spēkā
76941LVS CEN ISO/TS 7552-1:2024Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumour cells (CTCs) in venous whole blood - Part 1: Isolated RNA (ISO/TS 7552-1:2024)Standarts spēkā
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