Registration number (WIID)Project No.TitleStatus
76941LVS CEN ISO/TS 7552-1:2024Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumour cells (CTCs) in venous whole blood - Part 1: Isolated RNA (ISO/TS 7552-1:2024)Standarts spēkā
76940CEN ISO/TS 7552-2:2024Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumour cells (CTCs) in venous whole blood - Part 2: Isolated DNA (ISO/TS 7552-2:2024)Standarts spēkā
76940LVS CEN ISO/TS 7552-2:2024Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumour cells (CTCs) in venous whole blood - Part 2: Isolated DNA (ISO/TS 7552-2:2024)Standarts spēkā
75465LVS CEN/TS 17981-2:2023In vitro diagnostic Next Generation Sequencing (NGS) workflows - Part 2: Human RNA examinationStandarts spēkā
75465CEN/TS 17981-2:2023In vitro diagnostic Next Generation Sequencing (NGS) workflows - Part 2: Human RNA examinationStandarts 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
74322CEN ISO/TS 5798:2022In 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)Izstrādē
74138LVS CEN/TS 17981-1:2023In vitro diagnostic Next Generation Sequencing (NGS) workflows - Part 1: Human DNA examinationStandarts spēkā
74138CEN/TS 17981-1:2023In vitro diagnostic Next Generation Sequencing (NGS) workflows - Part 1: Human DNA examinationStandarts spēkā
73608prEN ISO 15194In vitro diagnostic medical devices - Requirements for certified reference materials and the content of supporting documentation (ISO/DIS 15194:2023)Izstrādē
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