Registration number (WIID)Project No.TitleStatus
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
69799ISO 20186-2:2019Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 2: Isolated genomic DNAStandarts 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
51984ISO 19001:2013In vitro diagnostic medical devices — Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biologyStandarts spēkā
83565ISO 21474-3:2024In vitro diagnostic medical devices — Multiplex molecular testing for nucleic acids — Part 3: Interpretation and reportsStandarts spēkā
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