Registration number (WIID)Project No.TitleStatus
38477ISO 15190:2003Medical laboratories -- Requirements for safetyAtcelts
73506ISO/TS 22583:2019Guidance for supervisors and operators of point-of-care testing (POCT) devicesAtcelts
35173ISO 22870:2006Point-of-care testing (POCT) — Requirements for quality and competenceAtcelts
38590ISO/TR 18112:2006Clinical laboratory testing and in vitro diagnostic test systems — In vitro diagnostic medical devices for professional use — Summary of regulatory requirements for information supplied by the manufacturerAtcelts
70960ISO 21474-1:2020In vitro diagnostic medical devices — Multiplex molecular testing for nucleic acids — Part 1: Terminology and general requirements for nucleic acid quality evaluationAtcelts
40988ISO 18113-5:2009In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 5: In vitro diagnostic instruments for self-testingAtcelts
40984ISO 18113-1:2009In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirementsAtcelts
81712ISO/TS 5798:2022In vitro diagnostic test systems — Requirements and recommendations for detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) by nucleic acid amplification methodsAtcelts
42641ISO 15189:2007Medical laboratories — Particular requirements for quality and competenceAtcelts
31718ISO 18153:2003In vitro diagnostic medical devices — Measurement of quantities in biological samples — Metrological traceability of values for catalytic concentration of enzymes assigned calibrators and control materialsAtcelts
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