CEN/TC 140
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
70932 | EN ISO 18113-4:2024 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2022) | Standarts spēkā |
68157 | EN ISO 15189:2022 | Medical laboratories - Requirements for quality and competence (ISO 15189:2022) | Standarts spēkā |
61690 | LVS EN ISO 20166-2:2019 | Molecular 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 |
62263 | EN ISO 17511:2021 | In vitro diagnostic medical devices - Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples (ISO 17511:2020) | Standarts spēkā |
61692 | LVS EN ISO 6710:2017 | Single-use containers for human venous blood specimen collection (ISO 6710:2017) | Standarts spēkā |
75465 | CEN/TS 17981-2:2023 | In vitro diagnostic Next Generation Sequencing (NGS) workflows - Part 2: Human RNA examination | Standarts spēkā |
70930 | EN ISO 18113-2:2024 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2022) | Standarts spēkā |
67445 | LVS CEN/TS 17688-2:2022 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for Fine Needle Aspirates (FNAs) - Part 2: Isolated proteins | Standarts spēkā |
70931 | EN ISO 18113-3:2024 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2022) | Standarts spēkā |
61390 | LVS EN ISO 15195:2019 | Laboratory medicine - Requirements for the competence of calibration laboratories using reference measurement procedures (ISO 15195:2018) | Standarts spēkā |
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