Registration number (WIID)Project No.TitleStatus
5107EN 13641:2002Elimination 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
26165prCEN ISO/TS 25680Medical laboratories - Calculation and expression of measurement uncertaintyIzstrādē
78630FprEN ISO 22367Medical laboratories - Application of risk management to medical laboratories (ISO/FDIS 22637:2026)Izstrādē
78864EN ISO 23640:2015/prA11In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagentsIzstrādē
29677prEN 1659In vitro diagnostic systems - Culture media for microbiology - Terms and definitionsIzstrādē
83075EN ISO 15195:2019/prA1Laboratory medicine — Requirements for the competence of calibration laboratories using reference measurement procedures — Amendment 1Izstrādē
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
67445CEN/TS 17688-2:2021Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for Fine Needle Aspirates (FNAs) - Part 2: Isolated proteinsIzstrādē
67448CEN/TS 17688-3:2021Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for Fine Needle Aspirates (FNAs) - Part 3: Isolated genomic DNAIzstrādē
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