Registration number (WIID)Project No.TitleStatus
71064LVS EN ISO 20916:2024In vitro diagnostic medical devices - Clinical performance studies using specimens from human subjects - Good study practice (ISO 20916:2019)Standarts spēkā
68157LVS EN ISO 15189:2023Medical laboratories - Requirements for quality and competence (ISO 15189:2022)Standarts spēkā
74322LVS CEN ISO/TS 5798:2023In vitro diagnostic test systems - Requirements and recommendations for detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) by nucleic acid amplification methods (ISO/TS 5798:2022)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
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
68157EN ISO 15189:2022Medical laboratories - Requirements for quality and competence (ISO 15189:2022)Standarts spēkā
79016LVS EN ISO 15189:2022/A11:2023Medical laboratories - Requirements for quality and competenceStandarts spēkā
65451LVS CEN/TS 17390-3:2020Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood - Part 3: Preparations for analytical CTC stainingStandarts spēkā
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
75465CEN/TS 17981-2:2023In vitro diagnostic Next Generation Sequencing (NGS) workflows - Part 2: Human RNA examinationStandarts spēkā
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