Registration number (WIID)Project No.TitleStatus
78630FprEN ISO 22367Medical laboratories - Application of risk management to medical laboratories (ISO/FDIS 22637:2026)Izstrādē
5089-Methods for the determination of performance of culture mediaIzstrādē
23416prEN ISO 20776-2Evaluation of performance of antimicrobial susceptibility devicesIzstrādē
5113LVS EN ISO 15195:2003Laboratory medicine - Requirements for reference measurement laboratoriesAtcelts
37590LVS EN ISO 18113-2:2012In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009)Atcelts
5073LVS EN 12286:2000 /A1In vitro diagnostic medical devices - Measurement of qiantities in samples of biological origin - Presentation of reference measurement proceduresAtcelts
5115LVS EN 12286:1998/A1:2000In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Presentation of reference measurement proceduresAtcelts
41047LVS CEN/TS 16826-2:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for snap frozen tissue - Part 2: Isolated proteinsAtcelts
23415EN ISO 20776-1:2006Clinical laboratory testing and in vitro diagnostic test systems - Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices - Part 1: Reference method for testing the in vitro activity of antimicrobial agents against rapidly growing aerobic bacteria involved in infectious diseases (ISO 20776-1:2006)Atcelts
62543LVS EN ISO 22870:2017Point-of-care testing (POCT) - Requirements for quality and competence (ISO 22870:2016)Atcelts
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