ISO/TC 212

Registration number (WIID)Project No.TitleStatus
69799ISO 20186-2:2019Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 2: Isolated genomic DNAStandarts spēkā
69824ISO 15195:2018Laboratory medicine — Requirements for the competence of calibration laboratories using reference measurement proceduresStandarts spēkā
69445ISO/TS 20914:2019Medical laboratories — Practical guidance for the estimation of measurement uncertaintyStandarts spēkā
59944ISO/TS 17518:2015Medical laboratories — Reagents for staining biological material — Guidance for usersStandarts 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
51984ISO 19001:2013In vitro diagnostic medical devices — Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biologyStandarts 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
87680ISO/TS 22583:2024Requirements and recommendations for supervisors and operators of point-of-care testing (POCT) equipmentStandarts spēkā
78110ISO 20184-3:2021Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for frozen tissue — Part 3: Isolated DNAStandarts 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
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