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
85349ISO 18704:2026Molecular in vitro diagnostic examinations — Requirements and recommendations for pre-examination processes for urine and other body fluids — Isolated cell-free DNAStandarts spēkā
70960ISO 21474-1:2020In vitro diagnostic medical devices — Multiplex molecular testing for nucleic acids — Part 1: Terminology and general requirements for nucleic acid quality evaluationStandarts 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
87680ISO/TS 22583:2024Requirements and recommendations for supervisors and operators of point-of-care testing (POCT) equipmentStandarts spēkā
77070ISO/TS 23824:2024Medical laboratories — Guidance on application of ISO 15189 in anatomic pathologyStandarts spēkā
72191ISO 15190:2020Medical laboratories — Requirements for safetyStandarts spēkā
87738ISO 22367:2026Medical laboratories — Application of risk management to medical laboratoriesStandarts spēkā
83565ISO 21474-3:2024In vitro diagnostic medical devices — Multiplex molecular testing for nucleic acids — Part 3: Interpretation and reportsStandarts spēkā
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