Registration number (WIID)Project No.TitleStatus
38477ISO 15190:2003Medical laboratories — Requirements for safetyAtcelts
40918ISO/TS 22367:2008Medical laboratories — Reduction of error through risk management and continual improvementAtcelts
38363ISO 15195:2003Laboratory medicine — Requirements for reference measurement laboratoriesAtcelts
71119ISO 22870:2016Point-of-care testing (POCT) — Requirements for quality and competenceAtcelts
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
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
74605ISO 23118:2021Molecular in vitro diagnostic examinations — Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasmaAtcelts
74800ISO 23162:2021Basic semen examination — Specification and test methodsAtcelts
53345ISO/TS 22367:2008/Cor 1:2009Medical laboratories — Reduction of error through risk management and continual improvement — Technical Corrigendum 1Atcelts
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
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