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
88418ISO 35001:2019/Amd 1:2024Biorisk management for laboratories and other related organisations — Amendment 1: Climate action changesStandarts spēkā
83565ISO 21474-3:2024In vitro diagnostic medical devices — Multiplex molecular testing for nucleic acids — Part 3: Interpretation and reportsStandarts spēkā
74800ISO 23162:2021Basic semen examination — Specification and test methodsStandarts spēkā
77070ISO/TS 23824:2024Medical laboratories — Guidance on application of ISO 15189 in anatomic pathologyStandarts spēkā
72191ISO 15190:2020Medical laboratories — Requirements for safetyStandarts spēkā
87680ISO/TS 22583:2024Requirements and recommendations for supervisors and operators of point-of-care testing (POCT) equipmentStandarts 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
69800ISO 20186-3:2019Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 3: Isolated circulating cell free DNA from plasmaStandarts spēkā
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