ISO/TC 212

Registration number (WIID)Project No.TitleStatus
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
69801ISO 20184-2:2018Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for frozen tissue — Part 2: Isolated proteinsStandarts spēkā
81506ISO 5649:2024Medical laboratories — Concepts and specifications for the design, development, implementation and use of laboratory-developed testsStandarts spēkā
71254ISO 22367:2020Medical laboratories — Application of risk management to medical laboratoriesStandarts 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
79378ISO 17593:2022Clinical laboratory testing and in vitro medical devices — Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapyStandarts 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
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
57706ISO/PRF 16782Clinical laboratory testing — Criteria for acceptable lots of dehydrated Mueller-Hinton agar and broth for antimicrobial susceptibility testingStandarts spēkā
69824ISO 15195:2018Laboratory medicine — Requirements for the competence of calibration laboratories using reference measurement proceduresStandarts spēkā
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