CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 25659 | LVS EN ISO 15189:2007 A | Medical laboratories - Particular requirements for quality and competence (ISO 15189:2007) | Atcelts |
| 26165 | prCEN ISO/TS 25680 | Medical laboratories - Calculation and expression of measurement uncertainty | Izstrādē |
| 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 |
| 26409 | LVS 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 | Atcelts |
| 27341 | EN ISO 15193:2009 | In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for content and presentation of reference measurement procedures (ISO/FDIS 15193:2009) | Izstrādē |
| 27341 | LVS EN ISO 15193:2009 | In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for content and presentation of reference measurement procedures (ISO 15193:2009) | Standarts spēkā |
| 27354 | EN ISO 15194:2009 | In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for certified reference materials and the content of supporting documentation (ISO/FDIS 15194:2009) | Izstrādē |
| 27354 | LVS EN ISO 15194:2009 | In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for certified reference materials and the content of supporting documentation (ISO 15194:2009) | Standarts spēkā |
| 27616 | EN ISO 18113-1:2009 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO/FDIS 18113-1:2009) | 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 |
Displaying 81-90 of 274 results.