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
60817LVS EN ISO 23640:2015In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)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
70355LVS EN ISO 20776-2:2022Clinical laboratory testing and in vitro diagnostic test systems - Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices - Part 2: Evaluation of performance of antimicrobial susceptibility test devices against reference broth micro-dilution (ISO 20776-2:2021)Standarts spēkā
68137LVS CEN/TS 17747:2022Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for exosomes and other extracellular vesicles in venous whole blood - DNA, RNA and proteinsStandarts spēkā
5107LVS EN 13641:2003Elimination or reduction of risk of infection related to in vitro diagnostic reagentsStandarts spēkā
22397LVS EN 13612:2003 /AC:2003Performance evaluation of in vitro diagnostic medical devicesStandarts spēkā
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
68065LVS EN ISO 23162:2021Basic semen examination - Specification and test methods (ISO 23162:2021)Standarts spēkā
70929EN 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
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