Registration number (WIID)Project No.TitleStatus
37589EN ISO 18113-1:2011In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009)Atcelts
5114LVS EN ISO 15189:2003 AMedical laboratories - Particular 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
67448CEN/TS 17688-3:2021Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for Fine Needle Aspirates (FNAs) - Part 3: Isolated genomic DNAAtcelts
33817EN ISO 15197:2013In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO/DIS 15197:2011)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/DIS 16256:2011)Atcelts
41043LVS CEN/TS 16945:2016Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for metabolomics in urine, venous blood serum and plasmaAtcelts
27620LVS EN ISO 18113-5:2010In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009)Atcelts
24023LVS EN ISO 15197:2003 /AC:2005In vitro diagnostic test systems - Requirements for blood- glucose monitoring systems for self-testing in managing diabetes mellitusAtcelts
5108LVS EN ISO 15197:2003In vitro diagnostic test systems - Requirements for blood- glucose monitoring systems for self-testing in managing diabetes mellitusAtcelts
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