Registration number (WIID)Project No.TitleStatus
26301ISO 15189:2003Medical laboratories — Particular requirements for quality and competenceAtcelts
40987ISO 18113-4:2009In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 4: In vitro diagnostic reagents for self-testingAtcelts
36872ISO 17593:2007Clinical laboratory testing and in vitro medical devices — Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapyAtcelts
38477ISO 15190:2003Medical laboratories — Requirements for safetyAtcelts
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
67021ISO/NP 17822-2In vitro diagnostic test systems — Qualitative nucleic acid-based in vitro examination procedures for detection and identification of microbial pathogens — Part 2: Sample preparation and nucleic acid extractionIzstrādē
Displaying 71-80 of 146 results.