CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 61693 | LVS EN ISO 20166-1:2019 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for formalin-fixed and paraffin-embedded (FFPE) tissue - Part 1: Isolated RNA (ISO 20166-1:2018) | Standarts spēkā |
| 74138 | LVS CEN/TS 17981-1:2023 | In vitro diagnostic Next Generation Sequencing (NGS) workflows - Part 1: Human DNA examination | Standarts spēkā |
| 5116 | LVS EN 12322:2001/A1:2002 | In vitro diagnostic medical devices - Culture media for microbiology - Performance criteria for culture media | Standarts spēkā |
| 67448 | LVS CEN/TS 17688-3:2022 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for Fine Needle Aspirates (FNAs) - Part 3: Isolated genomic DNA | Standarts spēkā |
| 5110 | LVS EN ISO 18153:2003 | In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability for catalytic concentration of enzymes assigned to calibrators and control materials | Standarts spēkā |
| 61687 | LVS EN ISO 20186-2:2019 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2: Isolated genomic DNA (ISO 20186-2:2019) | Standarts spēkā |
| 67446 | LVS CEN/TS 17626:2021 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for human specimen - Isolated microbiome DNA | Standarts spēkā |
| 70933 | LVS EN ISO 18113-5:2024 | In 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 |
| 70929 | LVS EN ISO 18113-1:2024 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions, and general requirements (ISO 18113-1:2022) | Standarts spēkā |
| 70931 | LVS 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 |
Displaying 261-270 of 282 results.