CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 70930 | EN ISO 18113-2:2024 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2022) | Standarts spēkā |
| 70932 | 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 |
| 61863 | 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/DIS 20776-1:2018) | Standarts spēkā |
| 61390 | EN ISO 15195:2019 | Laboratory medicine - Requirements for the competence of calibration laboratories using reference measurement procedures (ISO/DIS 15195:2018) | Standarts spēkā |
| 76940 | LVS 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 |
| 5109 | LVS EN 13532:2003 | General requirements for in vitro diagnostic medical devices for self-testing | 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 |
| 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 |
| 5111 | LVS EN 14136:2004 | Use of external quality assessment schemes in the assessment of the performance of in vitro diagnostic examination procedures | Standarts spēkā |
| 76942 | CEN ISO/TS 7552-3:2024 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumour cells (CTCs) in venous whole blood - Part 3: Preparations for analytical CTC staining (ISO/TS 7552-3:2024) | Standarts spēkā |
Displaying 211-220 of 282 results.