CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 37590 | EN ISO 18113-2:2011 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009) | Atcelts |
| 5102 | LVS EN 14820:2005 | Single-use containers for human venous blood specimen collection | Atcelts |
| 29669 | EN ISO 15189:2012 | Medical laboratories - Requirements for quality and competence (ISO/DIS 15189:2011) | Atcelts |
| 39727 | LVS EN ISO 23640:2013 | In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011) | Atcelts |
| 64590 | LVS CEN/TS 16826-3:2018 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for snap frozen tissue - Part 3: Isolated DNA | Atcelts |
| 41043 | LVS CEN/TS 16945:2016 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for metabolomics in urine, venous blood serum and plasma | Atcelts |
| 62239 | LVS CEN/TS 17305:2019 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for saliva - Isolated human DNA | Atcelts |
| 5104 | LVS EN 13640:2003 | Stability testing of in vitro diagnostic reagents | Atcelts |
| 33817 | EN ISO 15197:2013 | In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2013) | Atcelts |
| 37593 | EN ISO 18113-5:2011 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009) | Atcelts |
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