ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 69801 | ISO 20184-2:2018 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for frozen tissue — Part 2: Isolated proteins | Standarts spēkā |
| 76677 | ISO 15189:2022 | Medical laboratories — Requirements for quality and competence | Standarts spēkā |
| 87738 | ISO/DIS 22367 | Medical laboratories — Application of risk management to medical laboratories | Aptauja slēgta |
| 85349 | ISO/DIS 18704 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for urine and other body fluids — Isolated cell free DNA | Aptauja slēgta |
| 40918 | ISO/TS 22367:2008 | Medical laboratories — Reduction of error through risk management and continual improvement | 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 |
| 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 |
| 26301 | ISO 15189:2003 | Medical laboratories — Particular requirements for quality and competence | Atcelts |
| 26306 | ISO 15194:2002 | In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Description of reference materials | Atcelts |
| 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 |
Displaying 41-50 of 142 results.