Registration number (WIID)Project No.TitleStatus
5094EN 591:1994In vitro diagnostic systems - Requirements for user manuals for in vitro diagnostic instruments for professional useAtcelts
25659EN ISO 15189:2007Medical laboratories - Particular requirements for quality and competence (ISO 15189:2007)Atcelts
5108EN ISO 15197:2003In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2003)Atcelts
5101EN 592:2002Instructions for use for in vitro diagnostic instruments for self-testingAtcelts
5080EN 12376:1999In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biologyAtcelts
32667CEN ISO/TS 22367:2010Medical laboratories - Reduction of error through risk management and continual improvement (ISO/TS 22367:2008, including Cor 1:2009)Atcelts
24452EN ISO 22870:2006Point-of-care testing (POCT) - Requirements for quality and competence (ISO 22870:2006)Atcelts
24023EN ISO 15197:2003/AC:2005In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2003)Atcelts
5067EN 375:1992In vitro diagnostic systems - Requirements for labelling in vitro diagnostic reagents for professional useAtcelts
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
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