CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 37208 | LVS EN ISO 16256:2013 | Clinical 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 |
| 65450 | LVS CEN/TS 17390-1:2020 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood - Part 1: Isolated RNA | 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 |
| 41047 | CEN/TS 16826-2:2015 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for snap frozen tissue - Part 2: Isolated proteins | Atcelts |
| 24023 | EN ISO 15197:2003/AC:2005 | In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2003) | 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 |
| 29759 | EN ISO 23640:2011 | In vitro diagnostic medical devices - Stability testing of in vitro diagnostic reagents (ISO/DIS 23640:2009) | Atcelts |
| 37593 | EN ISO 18113-5:2011 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009) | Atcelts |
| 37591 | EN ISO 18113-3:2011 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009) | Atcelts |
| 5067 | LVS EN 375:1992 | In vitro diagnostic systems - Requirements for labelling in vitro diagnostic reagents for professional use | Atcelts |
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