ISO/TC 212

Registration number (WIID)Project No.TitleStatus
78024ISO 21474-2:2022In vitro diagnostic medical devices — Multiplex molecular testing for nucleic acids — Part 2: Validation and verificationStandarts 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
81506ISO 5649:2024Medical laboratories — Concepts and specifications for the design, development, implementation and use of laboratory-developed testsStandarts spēkā
79379ISO 16256:2021Clinical laboratory testing and in vitro diagnostic test systems — Broth micro-dilution reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infectious diseasesStandarts 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
69801ISO 20184-2:2018Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for frozen tissue — Part 2: Isolated proteinsStandarts spēkā
75442ISO 20166-4:2021Molecular in vitro diagnostic examinations — Specifications for preexamination processes for formalin-fixed and paraffin-embedded (FFPE) tissue — Part 4: In situ detection techniquesStandarts spēkā
67022ISO 17822:2020In vitro diagnostic test systems — Nucleic acid amplification-based examination procedures for detection and identification of microbial pathogens — Laboratory quality practice guideStandarts spēkā
88418ISO 35001:2019/Amd 1:2024Biorisk management for laboratories and other related organisations — Amendment 1: Climate action changesStandarts spēkā
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