Registration number (WIID)Project No.TitleStatus
81712ISO/TS 5798:2022In vitro diagnostic test systems — Requirements and recommendations for detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) by nucleic acid amplification methodsStandarts spēkā
69799ISO 20186-2:2019Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 2: Isolated genomic DNAStandarts spēkā
57706ISO/PRF 16782Clinical laboratory testing — Criteria for acceptable lots of dehydrated Mueller-Hinton agar and broth for antimicrobial susceptibility testingStandarts spēkā
84816ISO/TS 16766:2024Manufacturers’ considerations for in vitro diagnostic medical devices in a public health emergencyStandarts spēkā
79377ISO 20776-2:2021Clinical laboratory testing and in vitro diagnostic test systems — Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices — Part 2: Evaluation of performance of antimicrobial susceptibility test devices against reference broth micro-dilutionStandarts 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
69824ISO 15195:2018Laboratory medicine — Requirements for the competence of calibration laboratories using reference measurement proceduresStandarts 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
67217ISO 20186-1:2019Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 1: Isolated cellular RNAStandarts spēkā
69801ISO 20184-2:2018Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for frozen tissue — Part 2: Isolated proteinsStandarts spēkā
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