CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 5113 | LVS EN ISO 15195:2003 | Laboratory medicine - Requirements for reference measurement laboratories | Atcelts |
| 5114 | LVS EN ISO 15189:2003 A | Medical laboratories - Particular requirements for quality and competence | Atcelts |
| 5073 | LVS EN 12286:2000 /A1 | In vitro diagnostic medical devices - Measurement of qiantities in samples of biological origin - Presentation of reference measurement procedures | Atcelts |
| 65452 | CEN/TS 17390-2:2020 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood - Part 2: Isolated DNA. | Atcelts |
| 39727 | LVS EN ISO 23640:2013 | In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011) | Atcelts |
| 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 |
| 5098 | LVS EN 375:2001 | In vitro diagnostic systems - Requirements for labelling of in vitro diagnostic reagents for self-testing | Atcelts |
| 5095 | LVS EN 592:2001 | In vitro diagnostic systems - Requirements for user manuals for in vitro diagnostic instruments for home use | Atcelts |
| 5069 | EN 928:1995 | In vitro diagnostic systems - Guidance on the application of EN 29001 and EN 46001 and of EN 29002 and EN 46002 for in vitro diagnostic medical devices | Atcelts |
| 37592 | EN ISO 18113-4:2011 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009) | Atcelts |
Displaying 111-120 of 277 results.