Registration number (WIID)Project No.TitleStatus
71119ISO 22870:2016Point-of-care testing (POCT) — Requirements for quality and competenceAtcelts
35172ISO/TR 22869:2005Medical laboratories — Guidance on laboratory implementation of ISO 15189: 2003Atcelts
32050ISO 19001:2002In vitro diagnostic medical devices — Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biologyAtcelts
38477ISO 15190:2003Medical laboratories — Requirements for safetyAtcelts
40987ISO 18113-4:2009In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 4: In vitro diagnostic reagents for self-testingAtcelts
40985ISO 18113-2:2009In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 2: In vitro diagnostic reagents for professional useAtcelts
42022ISO 15194:2009In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Requirements for certified reference materials and the content of supporting documentationAtcelts
38477ISO 15190:2003Medical laboratories -- Requirements for safetyAtcelts
26306ISO 15194:2002In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Description of reference materialsAtcelts
40918ISO/TS 22367:2008Medical laboratories — Reduction of error through risk management and continual improvementAtcelts
Displaying 51-60 of 147 results.