CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 77454 | LVS 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) | |
| 78630 | LVS EN ISO 22367:2026 | Medical laboratories - Application of risk management to medical laboratories (ISO 22637:2026) | |
| 5097 | LVS EN 12322:1999 | In vitro diagnostic medical devices - Culture media for microbiology - Performance criteria for culture media | |
| 77643 | EN ISO 5649:2024 | Medical laboratories - Concepts and specifications for the design, development, implementation, and use of laboratory-developed tests (ISO 5649:2024) | Standarts spēkā |
| 76941 | CEN ISO/TS 7552-1:2024 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumour cells (CTCs) in venous whole blood - Part 1: Isolated RNA (ISO/TS 7552-1:2024) | 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 |
| 61686 | EN ISO 20186-3:2019 | Molecular in-vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 3: Isolated circulating cell free DNA from plasma (ISO 20186-3:2019) | 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 |
| 70929 | 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 |
| 61863 | LVS EN ISO 20776-1:2020 | Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices - Part 1: Broth micro-dilution reference method for testing the in vitro activity of antimicrobial agents against rapidly growing aerobic bacteria involved in infectious diseases (ISO 20776-1:2019, including Corrected version 2019-12) | Standarts spēkā |
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