ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 41630 | ISO 20776-1:2006 | Clinical laboratory testing and in vitro diagnostic test systems — Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices — Part 1: Reference method for testing the in vitro activity of antimicrobial agents against rapidly growing aerobic bacteria involved in infectious diseases | Atcelts |
| 38590 | ISO/TR 18112:2006 | Clinical laboratory testing and in vitro diagnostic test systems — In vitro diagnostic medical devices for professional use — Summary of regulatory requirements for information supplied by the manufacturer | Atcelts |
| 73506 | ISO/TS 22583:2019 | Guidance for supervisors and operators of point-of-care testing (POCT) devices | Atcelts |
| 31718 | ISO 18153:2003 | In vitro diagnostic medical devices — Measurement of quantities in biological samples — Metrological traceability of values for catalytic concentration of enzymes assigned calibrators and control materials | Atcelts |
| 40986 | ISO 18113-3:2009 | In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use | Atcelts |
| 42641 | ISO 15189:2007 | Medical laboratories — Particular requirements for quality and competence | Atcelts |
| 83899 | ISO/WD TS 8219 | Sequencing and clinical application to infectious diseases | Izstrādē |
| 42640 | ISO 15189:2003/DAmd 1 | Medical laboratories — Particular requirements for quality and competence — Amendment 1 | Izstrādē |
| 67177 | ISO/CD 20164 | Molecular in-vitro diagnostic examinations — Specifications for pre-examination processes for FFPE tissue — DNA | Izstrādē |
| 31449 | ISO/WD 17593 | Specifications and standards for instruments for self testing in monitoring of anticoagulation treatment | Izstrādē |
Displaying 71-80 of 142 results.