Registration number (WIID)Project No.TitleStatus
65451CEN/TS 17390-3:2020Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood - Part 3: Preparations for analytical CTC stainingAtcelts
5102LVS EN 14820:2005Single-use containers for human venous blood specimen collectionAtcelts
39727LVS EN ISO 23640:2013In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)Atcelts
27619LVS EN ISO 18113-4:2010In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009)Atcelts
5114LVS EN ISO 15189:2003 AMedical laboratories - Particular requirements for quality and competenceAtcelts
5073LVS EN 12286:2000In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Presentation of reference measurement proceduresAtcelts
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
65450CEN/TS 17390-1:2020Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood - Part 1: Isolated RNAAtcelts
26409LVS EN 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 devicesAtcelts
25659LVS EN ISO 15189:2007 AMedical laboratories - Particular requirements for quality and competence (ISO 15189:2007)Atcelts
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