Registration number (WIID)Project No.TitleStatus
5115EN 12286:1998/A1:2000In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Presentation of reference measurement proceduresAtcelts
24452EN ISO 22870:2006Point-of-care testing (POCT) - Requirements for quality and competence (ISO 22870:2006)Atcelts
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
5114EN ISO 15189:2003Medical laboratories - Particular requirements for quality and competence (ISO 15189:2003)Atcelts
37208EN ISO 16256:2012Clinical laboratory testing and in vitro diagnostic test systems - Reference method for testing the in vitro activity of antimicrobial agents against yeast of fungi involved in infectious diseases (ISO/DIS 16256:2011)Atcelts
23415LVS EN ISO 20776-1:2007Clinical 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 diseasesAtcelts
5074EN 12287:1999In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Description of reference materialsAtcelts
5098EN 375:2001Information supplied by the manufacturer with in vitro diagnostic reagents for professional useAtcelts
29669EN ISO 15189:2012Medical laboratories - Requirements for quality and competence (ISO/DIS 15189:2011)Atcelts
33817EN ISO 15197:2013In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO/DIS 15197:2011)Atcelts
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