Registration number (WIID)Project No.TitleStatus
32050ISO 19001:2002In vitro diagnostic medical devices — Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biologyAtcelts
69985ISO 21151:2020In vitro diagnostic medical devices — Requirements for international harmonisation protocols establishing metrological traceability of values assigned to calibrators and human samplesAtcelts
35172ISO/TR 22869:2005Medical laboratories Guidance on laboratory implementation of ISO 15189: 2003Atcelts
41630ISO 20776-1:2006Clinical laboratory testing and in vitro diagnostic test systems — Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices — Part 1: Reference method for testing the in vitro activity of antimicrobial agents against rapidly growing aerobic bacteria involved in infectious diseasesAtcelts
40985ISO 18113-2:2009In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 2: In vitro diagnostic reagents for professional useAtcelts
40988ISO 18113-5:2009In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 5: In vitro diagnostic instruments for self-testingAtcelts
69984ISO 17511:2020In vitro diagnostic medical devices — Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samplesAtcelts
36872ISO 17593:2007Clinical laboratory testing and in vitro medical devices — Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapyAtcelts
26301ISO 15189:2003Medical laboratories — Particular requirements for quality and competenceAtcelts
39751ISO 15198:2004Clinical laboratory medicine — In vitro diagnostic medical devices — Validation of user quality control procedures by the manufacturerAtcelts
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