ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 93489 | ISO/CD TS 16782 | Clinical laboratory testing — Criteria for acceptable lots of dehydrated Mueller-Hinton agar and broth for antimicrobial susceptibility testing | 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 | Requirements for the identification and characterisation of microbes using next generation sequencing direct from clinical specimens in the management of infectious disease | 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 slēgta |
| 87673 | ISO/DIS 24051-1 | Medical laboratories — Part 1: General principles for the application of artificial intelligence in medical laboratories | Aptauja slēgta |
| 90120 | ISO/DIS 25379-1 | In vitro diagnostic Next Generation Sequencing (NGS) workflows — Part 1: Human DNA examination | Izstrādē |
| 90121 | ISO/DIS 25379-2 | In vitro diagnostic Next Generation Sequencing (NGS) workflows — Part 2: Human RNA examination | Izstrādē |
Displaying 81-90 of 147 results.