CEN/TC 140
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
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 | LVS EN 928:2001 | 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 |
62543 | LVS EN ISO 22870:2017 | Point-of-care testing (POCT) - Requirements for quality and competence (ISO 22870:2016) | Atcelts |
29669 | LVS EN ISO 15189:2013 A | Medical laboratories - Requirements for quality and competence (ISO 15189:2012, Corrected version 2014-08-15) | Atcelts |
5100 | LVS EN 591:2001 | In vitro diagnostic systems - Requirements for user manuals for in vitro diagnostic instruments for professional use | Atcelts |
37590 | LVS EN ISO 18113-2:2012 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009) | Atcelts |
41047 | LVS CEN/TS 16826-2:2015 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for snap frozen tissue - Part 2: Isolated proteins | Atcelts |
41042 | LVS CEN/TS 16827-1:2015 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for FFPE tissue - Part 1: Isolated RNA | Atcelts |
5068 | LVS EN 376:2001 | In vitro diagnostic systems - Requirements for labelling of in vitro diagnostic reagents for self-testing | Atcelts |
Displaying 161-170 of 272 results.