Registration number (WIID)Project No.TitleStatus
75465LVS CEN/TS 17981-2:2023In vitro diagnostic Next Generation Sequencing (NGS) workflows - Part 2: Human RNA examinationStandarts spēkā
70929LVS EN ISO 18113-1:2024In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions, and general requirements (ISO 18113-1:2022)Standarts spēkā
5107LVS EN 13641:2003Elimination or reduction of risk of infection related to in vitro diagnostic reagentsStandarts spēkā
68157EN ISO 15189:2022Medical laboratories - Requirements for quality and competence (ISO/DIS 15189:2021)Standarts spēkā
70518LVS EN ISO 6717:2021In vitro diagnostic medical devices - Single-use containers for the collection of specimens from humans other than blood (ISO 6717:2021)Standarts spēkā
75465CEN/TS 17981-2:2023In vitro diagnostic Next Generation Sequencing (NGS) workflows - Part 2: Human RNA examinationStandarts spēkā
61690LVS EN ISO 20166-2:2019Molecular in vitro diagnostic examinations - Specifications for pre-examinations processes for formalin-fixed and paraffin-embedded (FFPE) tissue - Part 2: Isolated proteins (ISO 20166-2:2018)Standarts spēkā
68138LVS CEN/TS 17742:2022Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free RNA from plasmaStandarts spēkā
31365LVS EN ISO 19001:2013In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology (ISO 19001:2013)Standarts spēkā
5103LVS EN 13612:2003Performance evaluation of in vitro diagnostic medical devicesStandarts spēkā
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