CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 76942 | LVS 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 |
| 5107 | LVS EN 13641:2003 | Elimination or reduction of risk of infection related to in vitro diagnostic reagents | Standarts spēkā |
| 5109 | LVS EN 13532:2003 | General requirements for in vitro diagnostic medical devices for self-testing | Standarts spēkā |
| 60817 | LVS EN ISO 23640:2015 | In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011) | Standarts spēkā |
| 61694 | LVS EN ISO 20184-1:2019 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for frozen tissue - Part 1: Isolated RNA (ISO 20184-1:2018) | Standarts spēkā |
| 70517 | LVS EN ISO 20184-3:2021 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for frozen tissue - Part 3: Isolated DNA (ISO 20184-3:2021) | Standarts spēkā |
| 64279 | LVS EN ISO 22367:2020 | Medical laboratories - Application of risk management to medical laboratories (ISO 22367:2020) | Standarts spēkā |
| 22397 | LVS EN 13612:2003 /AC:2003 | Performance evaluation of in vitro diagnostic medical devices | Standarts spēkā |
| 76941 | LVS 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 |
| 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 |
Displaying 221-230 of 272 results.