ISO/TC 212
Reģistrācijas numurs (WIID) | Projekta Nr. | Nosaukums | Statuss |
---|---|---|---|
38477 | ISO 15190:2003 | Medicīnas laboratorijas - Drošuma prasības | Atcelts |
26309 | ISO 15197:2003 | Systèmes d'essais de diagnostic in vitro — Exigences relatives aux systèmes d'autosurveillance de la glycémie destinés à la prise en charge du diabète sucré | Atcelts |
26306 | ISO 15194:2002 | In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Description of reference materials | Atcelts |
26305 | ISO 15193:2002 | In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Presentation of reference measurement procedures | Atcelts |
26301 | ISO 15189:2003 | Laboratoires d'analyses de biologie médicale — Exigences particulières concernant la qualité et la compétence | 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 | Medicīnas laboratorijas. Norādījumi ISO 15189:2003 ieviešanai laboratorijā | 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 |
38477 | ISO 15190:2003 | Medical laboratories — Requirements for safety | Atcelts |
70960 | ISO 21474-1:2020 | In vitro diagnostic medical devices — Multiplex molecular testing for nucleic acids — Part 1: Terminology and general requirements for nucleic acid quality evaluation | Atcelts |
Attēlo no 81. līdz 90. no pavisam 142 ieraksta(-iem).