Registration number (WIID)Project No.TitleStatus
5098LVS EN 375:2001In vitro diagnostic systems - Requirements for labelling of in vitro diagnostic reagents for self-testingAtcelts
5095LVS EN 592:2001In vitro diagnostic systems - Requirements for user manuals for in vitro diagnostic instruments for home useAtcelts
5069LVS EN 928:2001In vitro diagnostic systems - Guidance on the application of EN 29001 and EN 46001 and of EN 29002 and EN 46002 for in vitro diagnostic medical devicesAtcelts
62543LVS EN ISO 22870:2017Point-of-care testing (POCT) - Requirements for quality and competence (ISO 22870:2016)Atcelts
29669LVS EN ISO 15189:2013 AMedical laboratories - Requirements for quality and competence (ISO 15189:2012, Corrected version 2014-08-15)Atcelts
5100LVS EN 591:2001In vitro diagnostic systems - Requirements for user manuals for in vitro diagnostic instruments 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
41047LVS CEN/TS 16826-2:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for snap frozen tissue - Part 2: Isolated proteinsAtcelts
41042LVS CEN/TS 16827-1:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for FFPE tissue - Part 1: Isolated RNAAtcelts
5068LVS EN 376:2001In vitro diagnostic systems - Requirements for labelling of in vitro diagnostic reagents for self-testingAtcelts
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