ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 40985 | ISO 18113-2:2009 | In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 2: In vitro diagnostic reagents for professional use | 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 |
| 40986 | ISO 18113-3:2009 | In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use | Atcelts |
| 39751 | ISO 15198:2004 | Clinical laboratory medicine — In vitro diagnostic medical devices — Validation of user quality control procedures by the manufacturer | Atcelts |
| 38363 | ISO 15195:2003 | Laboratory medicine — Requirements for reference measurement laboratories | Atcelts |
| 87738 | ISO/FDIS 22367 | Medical laboratories — Application of risk management to medical laboratories | Izstrādē |
| 88356 | ISO/CD TS 24883 | In Vitro Diagnostic Medical Devices: Lateral Flow Immunoassay for Rapid Diagnostic Testing– General Guidance for Manufacturers | Izstrādē |
| 90479 | ISO/CD 25459 | In vitro diagnostic medical devices — Requirements for determining commutability of certified reference materials used as secondary calibrators or trueness controls | Izstrādē |
| 87674 | ISO/CD 24051-2 | Medical laboratories — Part 2: Digital pathology and artificial intelligence (AI)-based image analysis | Izstrādē |
Displaying 71-80 of 146 results.