Registration number (WIID)Project No.TitleStatus
74138CEN/TS 17981-1:2023In vitro diagnostic Next Generation Sequencing (NGS) workflows - Part 1: Human DNA examinationStandarts spēkā
73608FprEN ISO 15194In vitro diagnostic medical devices - Requirements for certified reference materials and the content of supporting documentation (ISO/FDIS 15194:2026)Izstrādē
73607FprEN ISO 15193In vitro diagnostic medical devices - Requirements for reference measurement procedures (ISO/FDIS 15193:2026)Izstrādē
72992prEN ISO 20776-3Clinical laboratory testing and in vitro diagnostic test systems -- Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices -- Part 3: Discdiffusion agar reference method for testing the in vitro activity of antimicrobial agents against rapidly growing aerobic bacteria involved in infectious diseasesIzstrādē
72259EN ISO 4307:2021Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for saliva - Isolated human DNA (ISO/DIS 4307:2021)Izstrādē
72259LVS EN ISO 4307:2022Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for saliva - Isolated human DNA (ISO 4307:2021)Standarts 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
71064EN ISO 20916:2024In vitro diagnostic medical devices - Clinical performance studies using specimens from human subjects - Good study practice (ISO 20916:2019)Standarts spēkā
70933LVS EN ISO 18113-5:2024In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2022)Standarts spēkā
70933EN ISO 18113-5:2024In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2022)Standarts spēkā
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