ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 40984 | ISO 18113-1:2009 | In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirements | Atcelts |
| 40918 | ISO/TS 22367:2008 | Medical laboratories — Reduction of error through risk management and continual improvement | Atcelts |
| 39751 | ISO 15198:2004 | Clinical laboratory medicine — In vitro diagnostic medical devices — Validation of user quality control procedures by the manufacturer | Atcelts |
| 39737 | ISO/WD 20776 | Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility devices | Izstrādē |
| 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 |
Displaying 121-130 of 147 results.