Registration number (WIID)Project No.TitleStatus
67022ISO 17822:2020In vitro diagnostic test systems — Nucleic acid amplification-based examination procedures for detection and identification of microbial pathogens — Laboratory quality practice guideStandarts spēkā
76677ISO 15189:2022Medical laboratories — Requirements for quality and competenceStandarts spēkā
69445ISO/TS 20914:2019Medical laboratories — Practical guidance for the estimation of measurement uncertaintyStandarts spēkā
67217ISO 20186-1:2019Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 1: Isolated cellular RNAStandarts 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
79379ISO 16256:2021Clinical laboratory testing and in vitro diagnostic test systems — Broth micro-dilution reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infectious diseasesStandarts spēkā
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
54976ISO 15197:2013In vitro diagnostic test systems — Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitusStandarts spēkā
71293ISO 35001:2019Biorisk management for laboratories and other related organisationsStandarts spēkā
72141ISO/TS 16782:2016Clinical laboratory testing — Criteria for acceptable lots of dehydrated Mueller-Hinton agar and broth for antimicrobial susceptibility testingStandarts spēkā
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