CEN/TC 140
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
65451 | CEN/TS 17390-3:2020 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood - Part 3: Preparations for analytical CTC staining | Atcelts |
5114 | EN ISO 15189:2003 | Medical laboratories - Particular requirements for quality and competence (ISO 15189:2003) | Atcelts |
27618 | EN ISO 18113-3:2009 | In 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 |
24452 | LVS EN ISO 22870:2006 | Point-of-care testing (POCT) - Requirements for quality and competence | Atcelts |
64590 | LVS CEN/TS 16826-3:2018 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for snap frozen tissue - Part 3: Isolated DNA | Atcelts |
41045 | CEN/TS 16835-2:2015 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2: Isolated genomic DNA | Atcelts |
41041 | CEN/TS 16835-1:2015 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1: Isolated cellular RNA | Atcelts |
24452 | EN ISO 22870:2006 | Point-of-care testing (POCT) - Requirements for quality and competence (ISO 22870:2006) | Atcelts |
41046 | CEN/TS 16827-2:2015 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for FFPE tissue - Part 2: Isolated proteins | Atcelts |
39727 | EN ISO 23640:2013 | In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011) | Atcelts |
Displaying 101-110 of 272 results.