ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 32050 | ISO 19001:2002 | In vitro diagnostic medical devices — Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology | Atcelts |
| 56027 | ISO 16256:2012 | Clinical laboratory testing and in vitro diagnostic test systems — Reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infectious diseases | Atcelts |
| 40987 | ISO 18113-4:2009 | In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 4: In vitro diagnostic reagents for self-testing | Atcelts |
| 35172 | ISO/TR 22869:2005 | Medical laboratories — Guidance on laboratory implementation of ISO 15189: 2003 | Atcelts |
| 56115 | ISO 15189:2012 | Medical laboratories — Requirements for quality and competence | Atcelts |
| 40984 | ISO 18113-1:2009 | In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirements | Atcelts |
| 35173 | ISO 22870:2006 | Point-of-care testing (POCT) — Requirements for quality and competence | Atcelts |
| 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 146 results.