Registration number (WIID)Project No.TitleStatus
68789EN ISO 20166-4:2021Molecular in vitro diagnostic examinations - Specifications for preexamination processes for formalin-fixed and paraffin-embedded (FFPE) tissue - Part 4: In situ detection techniques (ISO/DIS 20166-4:2020)Izstrādē
83076prEN ISO 20776-1 revSusceptibility 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 diseasesIzstrādē
25090prEN ISO 15194In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Description of reference materialsIzstrādē
83075EN ISO 15195:2019/prA1Laboratory medicine — Requirements for the competence of calibration laboratories using reference measurement procedures — Amendment 1Izstrādē
22397EN 13612:2002/AC:2002Performance evaluation of in vitro diagnostic medical devicesIzstrādē
78864EN ISO 23640:2015/prA11In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagentsIzstrādē
78630FprEN ISO 22367Medical laboratories - Application of risk management to medical laboratories (ISO/FDIS 22637:2026)Izstrādē
61687EN ISO 20186-2:2019Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2: Isolated genomic DNA (ISO/DIS 20186-2:2016)Izstrādē
29868prEN 13641Elimination or reduction of risk of infection related to in vitro diagnostic reagentsIzstrādē
83299-In vitro diagnostic examinations — Specifications for pre-examination processes for human specimens for the detection of infectious pathogens — Viruses, bacteria, fungi and parasitesIzstrādē
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