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 |
| 26305 | ISO 15193:2002 | In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Presentation of reference measurement procedures | Atcelts |
| 26309 | ISO 15197:2003 | In vitro diagnostic test systems — Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus | Atcelts |
| 40984 | ISO 18113-1:2009 | In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirements | Atcelts |
| 26306 | ISO 15194:2002 | In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Description of reference materials | Atcelts |
| 38477 | ISO 15190:2003 | Medical laboratories -- Requirements for safety | Atcelts |
| 73506 | ISO/TS 22583:2019 | Guidance for supervisors and operators of point-of-care testing (POCT) devices | Atcelts |
| 35173 | ISO 22870:2006 | Point-of-care testing (POCT) — Requirements for quality and competence | Atcelts |
| 41630 | ISO 20776-1:2006 | Clinical laboratory testing and in vitro diagnostic test systems — Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices — Part 1: Reference method for testing the in vitro activity of antimicrobial agents against rapidly growing aerobic bacteria involved in infectious diseases | 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 |
Displaying 61-70 of 146 results.