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 |
| 5067 | LVS EN 375:1992 | In vitro diagnostic systems - Requirements for labelling in vitro diagnostic reagents for professional use | Atcelts |
| 27618 | LVS EN ISO 18113-3:2010 | 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 |
| 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 |
| 27620 | LVS EN ISO 18113-5:2010 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009) | 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 |
| 5102 | LVS EN 14820:2005 | Single-use containers for human venous blood specimen collection | Atcelts |
| 39727 | LVS EN ISO 23640:2013 | In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011) | Atcelts |
| 5114 | LVS EN ISO 15189:2003 A | Medical laboratories - Particular requirements for quality and competence | Atcelts |
| 5073 | LVS EN 12286:2000 | In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Presentation of reference measurement procedures | Atcelts |
Displaying 91-100 of 276 results.