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
79016EN ISO 15189:2022/A11:2023Medical laboratories - Requirements for quality and competenceStandarts 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
79016LVS EN ISO 15189:2022/A11:2023Medical laboratories - Requirements for quality and competenceStandarts spēkā
74138LVS CEN/TS 17981-1:2023In vitro diagnostic Next Generation Sequencing (NGS) workflows - Part 1: Human DNA examinationStandarts spēkā
68066LVS EN ISO 23118:2021Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma (ISO 23118:2021)Standarts spēkā
61685LVS EN ISO 20186-1:2019Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1: Isolated cellular RNA (ISO 20186-1:2019)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
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