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
5114EN ISO 15189:2003Medical laboratories - Particular requirements for quality and competence (ISO 15189:2003)Atcelts
27618EN ISO 18113-3:2009In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO/FDIS 18113-3:2009)Atcelts
24452LVS EN ISO 22870:2006Point-of-care testing (POCT) - Requirements for quality and competenceAtcelts
64590LVS CEN/TS 16826-3:2018Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for snap frozen tissue - Part 3: Isolated DNAAtcelts
41045CEN/TS 16835-2:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2: Isolated genomic DNAAtcelts
41041CEN/TS 16835-1:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1: Isolated cellular RNAAtcelts
24452EN ISO 22870:2006Point-of-care testing (POCT) - Requirements for quality and competence (ISO 22870:2006)Atcelts
41046CEN/TS 16827-2:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for FFPE tissue - Part 2: Isolated proteinsAtcelts
39727EN ISO 23640:2013In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)Atcelts
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