CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 5109 | LVS EN 13532:2003 | General requirements for in vitro diagnostic medical devices for self-testing | Standarts spēkā |
| 68138 | LVS CEN/TS 17742:2022 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free RNA from plasma | Standarts spēkā |
| 5106 | LVS EN 13975:2003 | Sampling procedures used for acceptance testing of in vitro diagnostic medical devices - Statistical aspects | Standarts spēkā |
| 71064 | LVS EN ISO 20916:2024 | In vitro diagnostic medical devices - Clinical performance studies using specimens from human subjects - Good study practice (ISO 20916:2019) | Standarts spēkā |
| 79016 | EN ISO 15189:2022/A11:2023 | Medical laboratories - Requirements for quality and competence | Standarts spēkā |
| 5107 | LVS EN 13641:2003 | Elimination or reduction of risk of infection related to in vitro diagnostic reagents | 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 |
| 27341 | LVS EN ISO 15193:2009 | In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for content and presentation of reference measurement procedures (ISO 15193:2009) | Standarts spēkā |
| 68066 | LVS EN ISO 23118:2021 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma (ISO 23118:2021) | Standarts spēkā |
| 70354 | LVS EN ISO 16256:2022 | Clinical laboratory testing and in vitro diagnostic test systems - Broth micro-dilution reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infectious diseases (ISO 16256:2021) | Standarts spēkā |
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