ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 38590 | ISO/TR 18112:2006 | Clinical laboratory testing and in vitro diagnostic test systems — In vitro diagnostic medical devices for professional use — Summary of regulatory requirements for information supplied by the manufacturer | Atcelts |
| 38477 | ISO 15190:2003 | Medical laboratories -- Requirements for safety | Atcelts |
| 38477 | ISO 15190:2003 | Medical laboratories — Requirements for safety | Atcelts |
| 38363 | ISO 15195:2003 | Laboratory medicine — Requirements for reference measurement laboratories | Atcelts |
| 36872 | ISO 17593:2007 | Clinical laboratory testing and in vitro medical devices — Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapy | Atcelts |
| 35173 | ISO 22870:2006 | 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 |
| 35172 | ISO/TR 22869:2005 | Medical laboratories — Guidance on laboratory implementation of ISO 15189: 2003 | Atcelts |
| 34111 | ISO/WD 20259 | In vitro diagnostic medical devices — Labelling and dissemination of product information for in vitro diagnostic products | Izstrādē |
| 32050 | ISO 19001:2002 | In vitro diagnostic medical devices — Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology | Atcelts |
Displaying 121-130 of 143 results.