ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 90120 | ISO/CD 25379-1 | In vitro diagnostic Next Generation Sequencing (NGS) workflows — Part 1: Human DNA examination | Izstrādē |
| 90121 | ISO/CD 25379-2 | In vitro diagnostic Next Generation Sequencing (NGS) workflows — Part 2: Human RNA examination | Izstrādē |
| 86739 | ISO/CD TS 21385 | Guidance for the implementation of emerging technology in 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 |
| 90994 | ISO/CD TS 25646 | In vitro diagnostic medical devices — Definition of analytical performance specifications for laboratory measurements based on medical requirements | Izstrādē |
| 83899 | ISO/CD TS 8219 | Sequencing and clinical application to infectious diseases | Izstrādē |
| 26302 | ISO/DIS 15190 | Medical laboratories — Requirements for safety | Izstrādē |
| 26307 | ISO/DIS 15195 | Clinical laboratory medicine — Requirements for reference measurement laboratories | Izstrādē |
| 26310 | ISO/DIS 15198 | Clinical laboratory medicine — In vitro diagnostic medical devices — Validation of manufacturer's recommendations for user quality control | Izstrādē |
| 89155 | ISO/DIS 23640 | In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents | Aptauja |
Displaying 81-90 of 146 results.