ISO/TC 212

Registration number (WIID)Project No.TitleStatus
67179ISO 20166-1:2018Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for formalin-fixed and paraffin-embedded (FFPE) tissue — Part 1: Isolated RNAStandarts 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
69801ISO 20184-2:2018Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for frozen tissue — Part 2: Isolated proteinsStandarts spēkā
69445ISO/TS 20914:2019Medical laboratories — Practical guidance for the estimation of measurement uncertaintyStandarts spēkā
69824ISO 15195:2018Laboratory medicine — Requirements for the competence of calibration laboratories using reference measurement proceduresStandarts spēkā
69455ISO 20916:2019In vitro diagnostic medical devices — Clinical performance studies using specimens from human subjects — Good study practiceStandarts spēkā
69984ISO 17511:2020In vitro diagnostic medical devices — Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samplesStandarts spēkā
57706ISO/PRF 16782Clinical laboratory testing — Criteria for acceptable lots of dehydrated Mueller-Hinton agar and broth for antimicrobial susceptibility testingStandarts spēkā
76677ISO 15189:2022Medical laboratories — Requirements for quality and competenceStandarts spēkā
42021ISO 15193:2009In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Requirements for content and presentation of reference measurement proceduresStandarts spēkā
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