ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 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 |
| 40984 | ISO 18113-1:2009 | In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirements | Atcelts |
| 41631 | ISO 20776-2:2007 | Clinical laboratory testing and in vitro diagnostic test systems — Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices — Part 2: Evaluation of performance of antimicrobial susceptibility test devices | 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 |
| 35173 | ISO 22870:2006 | Point-of-care testing (POCT) — Requirements for quality and competence | Atcelts |
| 68763 | ISO/TS 20658:2017 | Medical laboratories — Requirements for collection, transport, receipt, and handling of samples | 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 |
| 71119 | ISO 22870:2016 | Point-of-care testing (POCT) — Requirements for quality and competence | Atcelts |
| 42641 | ISO 15189:2007 | Medical laboratories — Particular requirements for quality and competence | Atcelts |
| 53345 | ISO/TS 22367:2008/Cor 1:2009 | Medical laboratories — Reduction of error through risk management and continual improvement — Technical Corrigendum 1 | Atcelts |
Displaying 71-80 of 146 results.