CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 68066 | EN ISO 23118:2021 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma (ISO/DIS 23118:2020) | Izstrādē |
| 73608 | EN ISO 15194:2026 | In vitro diagnostic medical devices - Requirements for certified reference materials and the content of supporting documentation (ISO/FDIS 15194:2026) | Izstrādē |
| 25229 | prCEN ISO/TS 22367 | Medical laboratories - Reduction of error through risk management and continual improvement | Izstrādē |
| 29673 | prEN ISO 15190 | Medical laboratories - Requirements for safety | Izstrādē |
| 29868 | prEN 13641 | Elimination or reduction of risk of infection related to in vitro diagnostic reagents | Izstrādē |
| 5103 | EN 13612:2002 | Performance evaluation of in vitro diagnostic medical devices | Izstrādē |
| 5106 | EN 13975:2003 | Sampling procedures used for acceptance testing of in vitro diagnostic medical devices - Statistical aspects | Izstrādē |
| 77416 | prCEN ISO/TS 18701 | Molecular in vitro diagnostic examinations - Specificationsfor pre-examination processes for human specimens - Isolated microbiome DNA | Izstrādē |
| 5097 | EN 12322:1999 | In vitro diagnostic medical devices - Culture media for microbiology - Performance criteria for culture media | Izstrādē |
| 77417 | prCEN ISO/TS 18702 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for exosomes and other extracellular vesicles in venous whole blood - DNA, RNA and proteins | Izstrādē |
Displaying 51-60 of 277 results.