Registration number (WIID)Project No.TitleStatus
56027ISO 16256:2012Clinical 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 diseasesAtcelts
69985ISO 21151:2020In vitro diagnostic medical devices — Requirements for international harmonisation protocols establishing metrological traceability of values assigned to calibrators and human samplesAtcelts
40986ISO 18113-3:2009In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional useAtcelts
30716ISO 17511:2003In vitro diagnostic medical devices — Measurement of quantities in biological samples — Metrological traceability of values assigned to calibrators and control materialsAtcelts
40918ISO/TS 22367:2008Medical laboratories — Reduction of error through risk management and continual improvementAtcelts
40985ISO 18113-2:2009In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 2: In vitro diagnostic reagents for professional useAtcelts
32050ISO 19001:2002In vitro diagnostic medical devices — Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biologyAtcelts
35172ISO/TR 22869:2005Medical laboratories — Guidance on laboratory implementation of ISO 15189: 2003Atcelts
35172ISO/TR 22869:2005Medical laboratories Guidance on laboratory implementation of ISO 15189: 2003Atcelts
39751ISO 15198:2004Clinical laboratory medicine — In vitro diagnostic medical devices — Validation of user quality control procedures by the manufacturerAtcelts
Displaying 71-80 of 142 results.