Registration number (WIID)Project No.TitleStatus
90479ISO/DIS 25459In vitro diagnostic medical devices — Requirements for determining commutability of certified reference materials used as secondary calibrators or trueness controlsAptauja
93488ISO 15195:2018/CD Amd 1Laboratory medicine — Requirements for the competence of calibration laboratories using reference measurement procedures — Amendment 1Aptauja
39751ISO 15198:2004Clinical laboratory medicine — In vitro diagnostic medical devices — Validation of user quality control procedures by the manufacturerAtcelts
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
74605ISO 23118:2021Molecular in vitro diagnostic examinations — Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasmaAtcelts
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
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
71119ISO 22870:2016Point-of-care testing (POCT) — Requirements for quality and competenceAtcelts
38363ISO 15195:2003Laboratory medicine — Requirements for reference measurement laboratoriesAtcelts
56115ISO 15189:2012Medical laboratories — Requirements for quality and competenceAtcelts
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