CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 31365 | EN ISO 19001:2013 | In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology (ISO/DIS 19001:2010) | Izstrādē |
| 78864 | EN ISO 23640:2015/prA11 | In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents | 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 |
| 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 |
| 25229 | prCEN ISO/TS 22367 | Medical laboratories - Reduction of error through risk management and continual improvement | Izstrādē |
| 77416 | prCEN ISO/TS 18701 | Molecular in vitro diagnostic examinations - Specificationsfor pre-examination processes for human specimens - Isolated microbiome DNA | Izstrādē |
| 29673 | prEN ISO 15190 | Medical laboratories - Requirements for safety | Izstrādē |
| 60768 | - | Haematology - Determination of the concentration of total haemoglobin in blood - Reference methods | Izstrādē |
| 73607 | FprEN ISO 15193 | In vitro diagnostic medical devices - Requirements for reference measurement procedures (ISO/FDIS 15193:2026) | Izstrādē |
| 26409 | EN ISO 20776-2:2007 | Clinical laboratory testing and in vitro diagnostic test systems - Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices - Part 2: Evaluation of performance of antimicrobial susceptibility test devices (ISO 20776-2:2007) | Atcelts |
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