Registration number (WIID)Project No.TitleStatus
60818EN ISO 15197:2015In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2013)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
70930EN ISO 18113-2:2024In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2022)Standarts 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/DIS 15189:2021)Standarts spēkā
5111LVS EN 14136:2004Use of external quality assessment schemes in the assessment of the performance of in vitro diagnostic examination proceduresStandarts 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
74138LVS CEN/TS 17981-1:2023In vitro diagnostic Next Generation Sequencing (NGS) workflows - Part 1: Human DNA examinationStandarts spēkā
76940CEN ISO/TS 7552-2:2024Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumour cells (CTCs) in venous whole blood - Part 2: Isolated DNA (ISO/TS 7552-2:2024)Standarts 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
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