CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 41046 | LVS CEN/TS 16827-2:2015 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for FFPE tissue - Part 2: Isolated proteins | Atcelts |
| 5114 | EN ISO 15189:2003 | Medical laboratories - Particular requirements for quality and competence (ISO 15189:2003) | Atcelts |
| 65452 | CEN/TS 17390-2:2020 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood - Part 2: Isolated DNA | Atcelts |
| 5073 | EN 12286:1998 | In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Presentation of reference measurement procedures | Atcelts |
| 27617 | LVS EN ISO 18113-2:2010 | 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 |
| 41043 | 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 | CEN/TS 17305:2019 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for saliva - Isolated human DNA | Atcelts |
| 27619 | EN ISO 18113-4:2009 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO/FDIS 18113-4:2009) | Atcelts |
| 27616 | LVS EN ISO 18113-1:2010 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009) | Atcelts |
| 29669 | EN ISO 15189:2012 | Medical laboratories - Requirements for quality and competence (ISO/DIS 15189:2011) | Atcelts |
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