CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 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 |
| 37591 | EN ISO 18113-3:2011 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009) | Atcelts |
| 62543 | EN ISO 22870:2016 | Point-of-care testing (POCT) - Requirements for quality and competence (ISO/FDIS 22870:2016) | Atcelts |
| 5068 | EN 376:1992 | In vitro diagnostic systems - Requirements for labelling in vitro diagnostic reagents for self-testing | Atcelts |
| 41042 | CEN/TS 16827-1:2015 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for FFPE tissue - Part 1: Isolated RNA | Atcelts |
| 5067 | LVS EN 375:1992 | In vitro diagnostic systems - Requirements for labelling in vitro diagnostic reagents for professional use | Atcelts |
| 32667 | LVS 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 |
| 5069 | EN 928:1995 | 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 |
| 37208 | LVS EN ISO 16256:2013 | Clinical laboratory testing and in vitro diagnostic test systems - Reference method for testing the in vitro activity of antimicrobial agents against yeast of fungi involved in infectious diseases (ISO 16256:2012) | Atcelts |
| 41044 | LVS CEN/TS 16827-3:2015 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for FFPE tissue - Part 3: Isolated DNA | Atcelts |
Displaying 131-140 of 275 results.