ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 67180 | ISO/CD 20167 | Molecular in-vitro diagnostic examinations — Specifications for pre-examination processes for frozen tissue — Extracted proteins | Izstrādē |
| 67216 | ISO/CD 20185 | Molecular in-vitro diagnostic examinations — Specifications for pre-examination processes for blood — Genomic DNA | Izstrādē |
| 89155 | ISO/CD 23640 | In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents | Izstrādē |
| 87673 | ISO/CD 24051-1.2 | Medical laboratories — Part 1: General principles for the application of artificial intelligence in medical laboratories | Izstrādē |
| 88357 | ISO/CD 24884 | Electronic Instructions for Use for In Vitro Diagnostic Medical Devices (Minimum required information and means of delivery) | 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 |
| 88356 | ISO/CD TS 24883 | Lateral flow immunoassay for rapid diagnostic testing — General guidance for manufacturers | 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 |
Displaying 71-80 of 142 results.