CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 41044 | CEN/TS 16827-3:2015 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for FFPE tissue - Part 3: Isolated DNA | 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 |
| 41041 | 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 |
| 41047 | CEN/TS 16826-2:2015 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for snap frozen tissue - Part 2: Isolated proteins | Atcelts |
| 41046 | CEN/TS 16827-2:2015 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for FFPE tissue - Part 2: Isolated proteins | Atcelts |
| 32667 | CEN ISO/TS 22367:2010 | Medical laboratories - Reduction of error through risk management and continual improvement (ISO/TS 22367:2008, including Cor 1:2009) | Atcelts |
| 24452 | EN ISO 22870:2006 | Point-of-care testing (POCT) - Requirements for quality and competence (ISO 22870:2006) | Atcelts |
| 39727 | EN ISO 23640:2013 | In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011) | Atcelts |
| 5067 | EN 375:1992 | In vitro diagnostic systems - Requirements for labelling in vitro diagnostic reagents for professional use | Atcelts |
| 5098 | EN 375:2001 | Information supplied by the manufacturer with in vitro diagnostic reagents for professional use | Atcelts |
Displaying 101-110 of 277 results.