ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 40986 | ISO 18113-3:2009 | In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use | Atcelts |
| 73506 | ISO/TS 22583:2019 | Guidance for supervisors and operators of point-of-care testing (POCT) devices | 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 |
| 26301 | ISO 15189:2003 | Medical laboratories — Particular requirements for quality and competence | Atcelts |
| 26305 | ISO 15193:2002 | In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Presentation of reference measurement procedures | Atcelts |
| 35173 | ISO 22870:2006 | Point-of-care testing (POCT) — Requirements for quality and competence | Atcelts |
| 38363 | ISO 15195:2003 | Laboratory medicine — Requirements for reference measurement laboratories | 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 |
| 26309 | ISO 15197:2003 | In vitro diagnostic test systems — Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus | Atcelts |
Displaying 61-70 of 147 results.