Registration number (WIID)Project No.TitleStatus
41044CEN/TS 16827-3:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for FFPE tissue - Part 3: Isolated DNAAtcelts
37592EN ISO 18113-4:2011In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009)Atcelts
41042CEN/TS 16827-1:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for FFPE tissue - Part 1: Isolated RNAAtcelts
41045CEN/TS 16835-2:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2: Isolated genomic DNAAtcelts
64279EN ISO 22367:2020Medical laboratories - Application of risk management to medical laboratories (ISO 22367:2020)Atcelts
62239LVS CEN/TS 17305:2019Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for saliva - Isolated human DNAAtcelts
65450LVS CEN/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
41040CEN/TS 16835-3:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 3: Isolated circulating cell free DNA from plasmaAtcelts
27616EN ISO 18113-1:2009In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO/FDIS 18113-1:2009)Atcelts
5102EN 14820:2004Single-use containers for human venous blood specimen collectionAtcelts
Displaying 111-120 of 277 results.