CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 78630 | EN ISO 22367:2026 | Medical laboratories - Application of risk management to medical laboratories (ISO/DIS 22637:2025) | Standarts spēkā |
| 77454 | EN ISO 18704:2026 | Molecular in vitro diagnostic examinations - Requirements and recommendations for pre-examination processes for urine and other body fluids - Isolated cell-free DNA (ISO 18704:2026) | Standarts spēkā |
| 61694 | EN ISO 20184-1:2018 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for frozen tissue - Part 1: Isolated RNA (ISO 20184-1:2018) | Standarts spēkā |
| 75465 | CEN/TS 17981-2:2023 | In vitro diagnostic Next Generation Sequencing (NGS) workflows - Part 2: Human RNA examination | 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 |
| 61692 | EN ISO 6710:2017 | Single-use containers for human venous blood specimen collection (ISO 6710:2017) | Standarts spēkā |
| 61692 | LVS EN ISO 6710:2017 | Single-use containers for human venous blood specimen collection (ISO 6710:2017) | 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 |
| 74322 | LVS CEN ISO/TS 5798:2023 | In 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 |
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