ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 71119 | ISO 22870:2016 | Point-of-care testing (POCT) — Requirements for quality and competence | Atcelts |
| 35172 | ISO/TR 22869:2005 | Medical laboratories — Guidance on laboratory implementation of ISO 15189: 2003 | Atcelts |
| 32050 | ISO 19001:2002 | In vitro diagnostic medical devices — Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology | Atcelts |
| 38477 | ISO 15190:2003 | Medical laboratories — Requirements for safety | Atcelts |
| 40987 | ISO 18113-4:2009 | In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 4: In vitro diagnostic reagents for self-testing | Atcelts |
| 40985 | ISO 18113-2:2009 | In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 2: In vitro diagnostic reagents for professional use | Atcelts |
| 42022 | 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 | Atcelts |
| 38477 | ISO 15190:2003 | Medical laboratories -- Requirements for safety | Atcelts |
| 26306 | ISO 15194:2002 | In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Description of reference materials | Atcelts |
| 40918 | ISO/TS 22367:2008 | Medical laboratories — Reduction of error through risk management and continual improvement | Atcelts |
Displaying 51-60 of 147 results.