ISO/TC 212

Registration number (WIID)Project No.TitleStatus
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
69803ISO 20166-3:2018Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for formalin-fixed and paraffin-embedded (FFPE) tissue — Part 3: Isolated DNAStandarts spēkā
69824ISO 15195:2018Laboratory medicine — Requirements for the competence of calibration laboratories using reference measurement proceduresStandarts spēkā
69984ISO 17511:2020In vitro diagnostic medical devices — Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samplesAtcelts
69985ISO 21151:2020In vitro diagnostic medical devices — Requirements for international harmonisation protocols establishing metrological traceability of values assigned to calibrators and human samplesAtcelts
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
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
71119ISO 22870:2016Point-of-care testing (POCT) — Requirements for quality and competenceAtcelts
71254ISO 22367:2020Medical laboratories — Application of risk management to medical laboratoriesStandarts spēkā
71293ISO 35001:2019Biorisk management for laboratories and other related organisationsStandarts spēkā
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