Registration number (WIID)Project No.TitleStatus
37591LVS EN ISO 18113-3:2012In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009)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
62239CEN/TS 17305:2019Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for saliva - Isolated human DNAAtcelts
41045CEN/TS 16835-2:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2: Isolated genomic DNAAtcelts
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
65452CEN/TS 17390-2:2020Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood - Part 2: Isolated DNA.Atcelts
64279EN ISO 22367:2020Medical laboratories - Application of risk management to medical laboratories (ISO 22367:2020)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
37589LVS EN ISO 18113-1:2012In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009)Atcelts
25659EN ISO 15189:2007Medical laboratories - Particular requirements for quality and competence (ISO 15189:2007)Atcelts
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