CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 68789 | LVS EN ISO 20166-4:2021 | Molecular in vitro diagnostic examinations - Specifications for preexamination processes for formalin-fixed and paraffin-embedded (FFPE) tissue - Part 4: In situ detection techniques (ISO 20166-4:2021) | Standarts spēkā |
| 5116 | EN 12322:1999/A1:2001 | In vitro diagnostic medical devices - Culture media for microbiology - Performance criteria for culture media | Standarts spēkā |
| 70933 | 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 |
| 68137 | LVS CEN/TS 17747:2022 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for exosomes and other extracellular vesicles in venous whole blood - DNA, RNA and proteins | Standarts spēkā |
| 68157 | LVS EN ISO 15189:2023 | Medical laboratories - Requirements for quality and competence (ISO 15189:2022) | Standarts spēkā |
| 61685 | EN ISO 20186-1:2019 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1: Isolated cellular RNA (ISO 20186-1:2019) | Standarts spēkā |
| 76940 | CEN ISO/TS 7552-2:2024 | Molecular 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 |
| 70355 | LVS EN ISO 20776-2:2022 | Clinical 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 |
| 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 |
| 70932 | LVS 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 |
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