CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 72259 | EN ISO 4307:2021 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for saliva - Isolated human DNA (ISO 4307:2021) | Izstrādē |
| 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) | Izstrādē |
| 25658 | EN ISO 15189:2003/prA1 | Medical laboratories - Particular requirements for quality and competence - Amendment 1 (ISO 15189:2003/DAM 1:2005) | Izstrādē |
| 73608 | prEN ISO 15194 | In vitro diagnostic medical devices - Requirements for certified reference materials and the content of supporting documentation (ISO/DIS 15194:2023) | Izstrādē |
| 60919 | prEN ISO 23640 rev | In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents | Izstrādē |
| 68789 | EN ISO 20166-4:2021 | Molecular in vitro diagnostic examinations - Specifications for preexamination processes for formalin-fixed and paraffin-embedded (FFPE) tissue - Part 4: In situ detection techniques (ISO 20166-4:2021) | Izstrādē |
| 25090 | prEN ISO 15194 | In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Description of reference materials | Izstrādē |
| 29869 | prEN 13532 | General requirements for in vitro diagnostic medical devices for self-testing | Izstrādē |
| 81156 | prEN ISO 15197 rev | In vitro diagnostic test systems — Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus | Izstrādē |
| 22397 | EN 13612:2002/AC:2002 | Performance evaluation of in vitro diagnostic medical devices | Izstrādē |
Displaying 231-240 of 272 results.