CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 5114 | EN ISO 15189:2003 | Medical laboratories - Particular requirements for quality and competence (ISO 15189:2003) | Atcelts |
| 37208 | EN ISO 16256:2012 | 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 |
| 26409 | EN ISO 20776-2:2007 | Clinical laboratory testing and in vitro diagnostic test systems - Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices - Part 2: Evaluation of performance of antimicrobial susceptibility test devices (ISO 20776-2:2007) | Atcelts |
| 23415 | EN ISO 20776-1:2006 | Clinical laboratory testing and in vitro diagnostic test systems - Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices - Part 1: Reference method for testing the in vitro activity of antimicrobial agents against rapidly growing aerobic bacteria involved in infectious diseases (ISO 20776-1:2006) | 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 |
| 29759 | EN ISO 23640:2011 | In vitro diagnostic medical devices - Stability testing of in vitro diagnostic reagents (ISO/DIS 23640:2009) | Atcelts |
| 5080 | EN 12376:1999 | In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology | Atcelts |
| 27616 | LVS EN ISO 18113-1:2010 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009) | Atcelts |
| 27617 | EN ISO 18113-2:2009 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO/FDIS 18113-2:2009) | Atcelts |
| 62239 | CEN/TS 17305:2019 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for saliva - Isolated human DNA | Atcelts |
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