ISO/TC 212
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
68763 | ISO/TS 20658:2017 | Medical laboratories — Requirements for collection, transport, receipt, and handling of samples | Atcelts |
73506 | ISO/TS 22583:2019 | Guidance for supervisors and operators of point-of-care testing (POCT) devices | Atcelts |
38477 | ISO 15190:2003 | Medical laboratories -- Requirements for safety | Atcelts |
26309 | ISO 15197:2003 | In vitro diagnostic test systems — Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus | Atcelts |
26306 | ISO 15194:2002 | In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Description of reference materials | Atcelts |
26305 | ISO 15193:2002 | In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Presentation of reference measurement procedures | Atcelts |
26301 | ISO 15189:2003 | Medical laboratories — Particular requirements for quality and competence | 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 |
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 |
38477 | ISO 15190:2003 | Medical laboratories — Requirements for safety | Atcelts |
Displaying 81-90 of 142 results.