Registration number (WIID)Project No.TitleStatus
84816ISO/TS 16766:2024Manufacturers’ considerations for in vitro diagnostic medical devices in a public health emergencyStandarts spēkā
69801ISO 20184-2:2018Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for frozen tissue — Part 2: Isolated proteinsStandarts 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
69985ISO 21151:2020In vitro diagnostic medical devices — Requirements for international harmonisation protocols establishing metrological traceability of values assigned to calibrators and human samplesStandarts 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
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
59944ISO/TS 17518:2015Medical laboratories — Reagents for staining biological material — Guidance for usersStandarts 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
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
67215ISO 20184-1:2018Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for frozen tissue — Part 1: Isolated RNAStandarts spēkā
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