ISO/TC 212
| Reģistrācijas numurs (WIID) | Projekta Nr. | Nosaukums | Statuss |
|---|---|---|---|
| 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 |
| 38477 | ISO 15190:2003 | Medical laboratories — Requirements for safety | Atcelts |
| 36872 | ISO 17593:2007 | Clinical laboratory testing and in vitro medical devices — Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapy | Atcelts |
| 38363 | ISO 15195:2003 | Laboratory medicine — Requirements for reference measurement laboratories | Atcelts |
| 53345 | ISO/TS 22367:2008/Cor 1:2009 | Laboratoires médicaux — Réduction d'erreurs par gestion du risque et amélioration continue — Rectificatif technique 1 | Atcelts |
| 26305 | ISO 15193:2002 | In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Presentation of reference measurement procedures | Atcelts |
| 69985 | ISO 21151:2020 | In vitro diagnostic medical devices — Requirements for international harmonisation protocols establishing metrological traceability of values assigned to calibrators and human samples | Atcelts |
| 26306 | ISO 15194:2002 | In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Description of reference materials | Atcelts |
| 26301 | ISO 15189:2003 | Laboratoires d'analyses de biologie médicale — Exigences particulières concernant la qualité et la compétence | Atcelts |
| 38477 | ISO 15190:2003 | Medicīnas laboratorijas - Drošuma prasības | Atcelts |
Attēlo no 51. līdz 60. no pavisam 142 ieraksta(-iem).