CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 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 |
| 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 |
| 5068 | LVS EN 376:2001 | In vitro diagnostic systems - Requirements for labelling of in vitro diagnostic reagents for self-testing | Atcelts |
| 5100 | LVS EN 591:2001 | In vitro diagnostic systems - Requirements for user manuals for in vitro diagnostic instruments for professional use | Atcelts |
| 5105 | LVS EN ISO 17511:2003 | In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability of values assigned to calibrators and control materials | Atcelts |
| 5073 | LVS EN 12286:2000 /A1 | In vitro diagnostic medical devices - Measurement of qiantities in samples of biological origin - Presentation of reference measurement procedures | Atcelts |
| 24452 | LVS EN ISO 22870:2006 | Point-of-care testing (POCT) - Requirements for quality and competence | 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 |
| 41045 | CEN/TS 16835-2:2015 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2: Isolated genomic DNA | Atcelts |
| 64279 | EN ISO 22367:2020 | Medical laboratories - Application of risk management to medical laboratories (ISO 22367:2020) | Atcelts |
Displaying 91-100 of 277 results.