Registration number (WIID)Project No.TitleStatus
31365EN ISO 19001:2013In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology (ISO/DIS 19001:2010)Izstrādē
61695EN ISO 20184-2:2018Molecular in-vitro diagnostic examinations - Specifications for pre-examination processes for frozen tissue - Part 2: Isolated proteins (ISO/DIS 20184-2:2016)Izstrādē
70517EN ISO 20184-3:2021Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for frozen tissue - Part 3: Isolated DNA (ISO/DIS 20184-3:2020)Izstrādē
81156prEN ISO 15197 revIn vitro diagnostic test systems — Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitusIzstrādē
81454prEN ISO 25379-1In vitro diagnostic Next Generation Sequencing (NGS) workflows -- Part 1: Part 1: Human DNA examinationIzstrādē
78864EN ISO 23640:2015/prA11In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagentsIzstrādē
68066EN ISO 23118:2021Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma (ISO/DIS 23118:2020)Izstrādē
27341EN ISO 15193:2009In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for content and presentation of reference measurement procedures (ISO/FDIS 15193:2009)Izstrādē
39676-Molecular in-vitro diagnostic examinations - Specifications for pre-examination processes for selected types of sampleIzstrādē
70355EN ISO 20776-2:2022Clinical laboratory testing and in vitro diagnostic test systems - Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test - Part 2: Evaluation of performance of antimicrobial susceptibility test devices against reference broth micro-dilution (ISO/DIS 20776-2:2021)Izstrādē
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