Registration number (WIID)Project No.TitleStatus
29759EN ISO 23640:2011In vitro diagnostic medical devices - Stability testing of in vitro diagnostic reagents (ISO/DIS 23640:2009)Atcelts
5115LVS EN 12286:1998/A1:2000In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Presentation of reference measurement proceduresAtcelts
26409EN ISO 20776-2:2007Clinical laboratory testing and in vitro diagnostic test systems - Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices - Part 2: Evaluation of performance of antimicrobial susceptibility test devices (ISO 20776-2:2007)Atcelts
37592LVS EN ISO 18113-4:2012In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009)Atcelts
62543EN ISO 22870:2016Point-of-care testing (POCT) - Requirements for quality and competence (ISO 22870:2016)Atcelts
41033LVS CEN/TS 16826-1:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for snap frozen tissue - Part 1: Isolated RNAAtcelts
41046LVS CEN/TS 16827-2:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for FFPE tissue - Part 2: Isolated proteinsAtcelts
5114EN ISO 15189:2003Medical laboratories - Particular requirements for quality and competence (ISO 15189:2003)Atcelts
5112LVS EN 14254:2004In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humansAtcelts
62239CEN/TS 17305:2019Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for saliva - Isolated human DNAAtcelts
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