CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 61687 | EN ISO 20186-2:2019 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2: Isolated genomic DNA (ISO/DIS 20186-2:2016) | Izstrādē |
| 62240 | - | Quality assurance of POCT results - Assessment criteria for comparison measurement and implementation | Izstrādē |
| 60768 | - | Haematology - Determination of the concentration of total haemoglobin in blood - Reference methods | Izstrādē |
| 60919 | prEN ISO 23640 rev | In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents | Izstrādē |
| 5109 | EN 13532:2002 | General requirements for in vitro diagnostic medical devices for self-testing | Izstrādē |
| 23416 | prEN ISO 20776-2 | Evaluation of performance of antimicrobial susceptibility devices | Izstrādē |
| 74322 | CEN ISO/TS 5798:2022 | 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) | Izstrādē |
| 61690 | EN ISO 20166-2:2018 | Molecular in vitro diagnostic examinations - Specifications for pre-examinations processes for formalin-fixed and paraffin-embedded (FFPE) tissue - Part 2: Isolated proteins (ISO/DIS 20166-2:2016) | Izstrādē |
| 61695 | EN ISO 20184-2:2018 | Molecular in-vitro diagnostic examinations - Specifications for pre-examination processes for frozen tissue - Part 2: Isolated proteins (ISO/DIS 20184-2:2016) | Izstrādē |
| 70518 | EN ISO 6717:2021 | In vitro diagnostic medical devices - Single-use containers for the collection of specimens, other than blood, from humans (ISO/DIS 6717:2020) | Izstrādē |
Displaying 31-40 of 282 results.