Registration number (WIID)Project No.TitleStatus
41042CEN/TS 16827-1:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for FFPE tissue - Part 1: Isolated RNAAtcelts
5068EN 376:1992In vitro diagnostic systems - Requirements for labelling in vitro diagnostic reagents for self-testingAtcelts
5094EN 591:1994In vitro diagnostic systems - Requirements for user manuals for in vitro diagnostic instruments for professional useAtcelts
5104EN 13640:2002Stability testing of in vitro diagnostic reagentsAtcelts
62543EN ISO 22870:2016Point-of-care testing (POCT) - Requirements for quality and competence (ISO/FDIS 22870:2016)Atcelts
5099LVS EN 376:2003Information supplied by the manufacturer with in vitro diagnostic reagents for self-testingAtcelts
32667CEN ISO/TS 22367:2010Medical laboratories - Reduction of error through risk management and continual improvement (ISO/TS 22367:2008, including Cor 1:2009)Atcelts
29759EN ISO 23640:2011In vitro diagnostic medical devices - Stability testing of in vitro diagnostic reagents (ISO/DIS 23640:2009)Atcelts
24452EN ISO 22870:2006Point-of-care testing (POCT) - Requirements for quality and competence (ISO 22870:2006)Atcelts
5115EN 12286:1998/A1:2000In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Presentation of reference measurement proceduresAtcelts
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