Registration number (WIID)Project No.TitleStatus
56115ISO 15189:2012Medical laboratories — Requirements for quality and competenceAtcelts
40988ISO 18113-5:2009In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 5: In vitro diagnostic instruments for self-testingAtcelts
40986ISO 18113-3:2009In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional useAtcelts
71254ISO 22367:2020Medical laboratories — Application of risk management to medical laboratoriesAtcelts
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
41631ISO 20776-2:2007Clinical laboratory testing and in vitro diagnostic test systems — Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices — Part 2: Evaluation of performance of antimicrobial susceptibility test devicesAtcelts
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
74605ISO 23118:2021Molecular in vitro diagnostic examinations — Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasmaAtcelts
67026ISO/PWI 20093Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for blood — Cellular RNAIzstrādē
90120ISO/CD 25379-1In vitro diagnostic Next Generation Sequencing (NGS) workflows — Part 1: Human DNA examinationIzstrādē
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