Registration number (WIID)Project No.TitleStatus
5112LVS EN 14254:2004In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humansAtcelts
41041LVS CEN/TS 16835-1:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1: Isolated cellular RNAAtcelts
5067LVS EN 375:1992In vitro diagnostic systems - Requirements for labelling in vitro diagnostic reagents for professional useAtcelts
32667LVS CEN ISO/TS 22367:2010Medical laboratories - Reduction of error through risk management and continual improvement (ISO/TS 22367:2008, including Cor 1:2009)Atcelts
5069EN 928:1995In 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
37208LVS EN ISO 16256:2013Clinical 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 16256:2012)Atcelts
5113LVS EN ISO 15195:2003Laboratory medicine - Requirements for reference measurement laboratoriesAtcelts
33817LVS EN ISO 15197:2013In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2013)Atcelts
41040LVS CEN/TS 16835-3:2016Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 3: Isolated circulating cell free DNA from plasmaAtcelts
29759LVS EN ISO 23640:2012In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)Atcelts
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