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 |
| 30716 | ISO 17511:2003 | In vitro diagnostic medical devices — Measurement of quantities in biological samples — Metrological traceability of values assigned to calibrators and control materials | Atcelts |
| 40918 | ISO/TS 22367:2008 | Medical laboratories — Reduction of error through risk management and continual improvement | 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 |
| 32050 | ISO 19001:2002 | In vitro diagnostic medical devices — Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology | Atcelts |
| 35172 | ISO/TR 22869:2005 | Medical laboratories — Guidance on laboratory implementation of ISO 15189: 2003 | Atcelts |
| 35172 | ISO/TR 22869:2005 | Medical laboratories Guidance on laboratory implementation of ISO 15189: 2003 | Atcelts |
| 39751 | ISO 15198:2004 | Clinical laboratory medicine — In vitro diagnostic medical devices — Validation of user quality control procedures by the manufacturer | Atcelts |
| 40988 | ISO 18113-5:2009 | In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 5: In vitro diagnostic instruments for self-testing | Atcelts |
| 68763 | ISO/TS 20658:2017 | Medical laboratories — Requirements for collection, transport, receipt, and handling of samples | Atcelts |
Displaying 71-80 of 146 results.