Registration number (WIID)Project No.TitleStatus
68137CEN/TS 17747:2022Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for exosomes and other extracellular vesicles in venous whole blood - DNA, RNA and proteinsIzstrādē
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
78864EN ISO 23640:2015/prA11In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagentsIzstrādē
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
84410prCEN ISO/TS 17849Guidance on the validation and verification of quantitative and qualitative methodsIzstrādē
67445CEN/TS 17688-2:2021Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for Fine Needle Aspirates (FNAs) - Part 2: Isolated proteinsIzstrādē
78870EN ISO 15197:2015/prA11In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitusIzstrādē
5111EN 14136:2004Use of external quality assessment schemes in the assessment of the performance of in vitro diagnostic examination proceduresIzstrādē
39676-Molecular in-vitro diagnostic examinations - Specifications for pre-examination processes for selected types of sampleIzstrādē
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