CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 61692 | EN ISO 6710:2017 | Single-use containers for venous blood specimen collection (ISO/DIS 6710:2016) | Izstrādē |
| 72992 | prEN ISO 20776-3 | Clinical laboratory testing and in vitro diagnostic test systems -- Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices -- Part 3: Discdiffusion agar reference method for testing the in vitro activity of antimicrobial agents against rapidly growing aerobic bacteria involved in infectious diseases | Izstrādē |
| 26165 | prCEN ISO/TS 25680 | Medical laboratories - Calculation and expression of measurement uncertainty | Izstrādē |
| 61691 | EN ISO 20166-3:2019 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for formalin-fixed and paraffin-embedded (FFPE) tissue - Part 3: Isolated DNA (ISO/DIS 20166-3:2016) | Izstrādē |
| 5110 | EN ISO 18153:2003 | In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability of values for catalytic concentration of enzymes assigned to calibrators and control materials (ISO 18153:2003) | Izstrādē |
| 29677 | prEN 1659 | In vitro diagnostic systems - Culture media for microbiology - Terms and definitions | Izstrādē |
| 41042 | CEN/TS 16827-1:2015 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for FFPE tissue - Part 1: Isolated RNA | Atcelts |
| 5068 | EN 376:1992 | In vitro diagnostic systems - Requirements for labelling in vitro diagnostic reagents for self-testing | Atcelts |
| 5095 | EN 592:1994 | In vitro diagnostic systems - Requirements for user manuals for in vitro diagnostic instruments for home use | Atcelts |
| 62543 | EN ISO 22870:2016 | Point-of-care testing (POCT) - Requirements for quality and competence (ISO/FDIS 22870:2016) | Atcelts |
Displaying 71-80 of 275 results.