Registration number (WIID)Project No.TitleStatus
5098EN 375:2001Information supplied by the manufacturer with in vitro diagnostic reagents for professional useAtcelts
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
27620EN ISO 18113-5:2009In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO/FDIS 18113-5:2009)Atcelts
29669EN ISO 15189:2012Medical laboratories - Requirements for quality and competence (ISO/DIS 15189:2011)Atcelts
41047LVS CEN/TS 16826-2:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for snap frozen tissue - Part 2: Isolated proteinsAtcelts
41043LVS CEN/TS 16945:2016Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for metabolomics in urine, venous blood serum and plasmaAtcelts
27617EN ISO 18113-2:2009In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO/FDIS 18113-2:2009)Atcelts
37208EN ISO 16256:2012Clinical 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
41043CEN/TS 16945:2016Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for metabolomics in urine, venous blood serum and plasmaAtcelts
37590LVS EN ISO 18113-2:2012In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009)Atcelts
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