CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 27354 | EN ISO 15194:2009 | In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for certified reference materials and the content of supporting documentation (ISO 15194:2009) | 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 |
| 32667 | CEN ISO/TS 22367:2010 | Medical laboratories - Reduction of error through risk management and continual improvement (ISO/TS 22367:2008, including Cor 1:2009) | Atcelts |
| 41045 | LVS CEN/TS 16835-2:2016 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2: Isolated genomic DNA | Atcelts |
| 5094 | EN 591:1994 | In vitro diagnostic systems - Requirements for user manuals for in vitro diagnostic instruments for professional use | Atcelts |
| 27620 | EN ISO 18113-5:2009 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO/FDIS 18113-5:2009) | Atcelts |
| 5104 | EN 13640:2002 | Stability testing of in vitro diagnostic reagents | Atcelts |
| 5098 | EN 375:2001 | Information supplied by the manufacturer with in vitro diagnostic reagents for professional use | Atcelts |
| 5075 | EN 829:1996 | In vitro diagnostic systems - Transport packages for medical and biological specimens - Requirements, tests | Atcelts |
| 39727 | EN ISO 23640:2013 | In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011) | Atcelts |
Displaying 111-120 of 282 results.