ISO/TC 212

Registration number (WIID)Project No.TitleStatus
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
76677ISO 15189:2022Medical laboratories — Requirements for quality and competenceStandarts spēkā
59944ISO/TS 17518:2015Medical laboratories — Reagents for staining biological material — Guidance for usersStandarts spēkā
69445ISO/TS 20914:2019Medical laboratories — Practical guidance for the estimation of measurement uncertaintyStandarts spēkā
78024ISO 21474-2:2022In vitro diagnostic medical devices — Multiplex molecular testing for nucleic acids — Part 2: Validation and verificationStandarts 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
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
83565ISO 21474-3:2024In vitro diagnostic medical devices — Multiplex molecular testing for nucleic acids — Part 3: Interpretation and reportsStandarts spēkā
70464ISO 20776-1:2019Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices — Part 1: Broth micro-dilution reference method for testing the in vitro activity of antimicrobial agents against rapidly growing aerobic bacteria involved in infectious diseasesStandarts spēkā
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