Registration number (WIID)Project No.TitleStatus
26301ISO 15189:2003Medical laboratories — Particular requirements for quality and competenceAtcelts
87738ISO/DIS 22367Medical laboratories — Application of risk management to medical laboratoriesAptauja
85349ISO/DIS 18704Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for urine and other body fluids — Isolated cell free DNAAptauja slēgta
78110ISO 20184-3:2021Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for frozen tissue — Part 3: Isolated DNAStandarts spēkā
69802ISO 20166-2:2018Molecular in vitro diagnostic examinations — Specifications for pre-examinations processes for formalin-fixed and paraffin-embedded (FFPE) tissue — Part 2: Isolated proteinsStandarts spēkā
79377ISO 20776-2:2021Clinical 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 devices against reference broth micro-dilutionStandarts spēkā
51984ISO 19001:2013In vitro diagnostic medical devices — Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biologyStandarts spēkā
67217ISO 20186-1:2019Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 1: Isolated cellular RNAStandarts spēkā
69800ISO 20186-3:2019Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 3: Isolated circulating cell free DNA from plasmaStandarts spēkā
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 documentationStandarts spēkā
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