CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 62239 | CEN/TS 17305:2019 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for saliva - Isolated human DNA | Atcelts |
| 41041 | LVS CEN/TS 16835-1:2015 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1: Isolated cellular RNA | Atcelts |
| 5069 | LVS EN 928:2001 | In vitro diagnostic systems - Guidance on the application of EN 29001 and EN 46001 and of EN 29002 and EN 46002 for in vitro diagnostic medical devices | Atcelts |
| 5068 | LVS EN 376:2001 | In vitro diagnostic systems - Requirements for labelling of in vitro diagnostic reagents for self-testing | Atcelts |
| 37592 | LVS EN ISO 18113-4:2012 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009) | Atcelts |
| 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 |
| 5098 | EN 375:2001 | Information supplied by the manufacturer with in vitro diagnostic reagents for professional use | Atcelts |
| 37592 | EN ISO 18113-4:2011 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009) | Atcelts |
| 5115 | LVS EN 12286:1998/A1:2000 | In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Presentation of reference measurement procedures | Atcelts |
| 5098 | LVS EN 375:2001 | In vitro diagnostic systems - Requirements for labelling of in vitro diagnostic reagents for self-testing | Atcelts |
Displaying 101-110 of 275 results.