ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 91317 | ISO/AWI TS 25725 | Design and workflow requirements for in vitro diagnostics NGS based oncology application | Izstrādē |
| 88356 | ISO/CD TS 24883 | Lateral flow immunoassay for rapid diagnostic testing — General guidance for manufacturers | Izstrādē |
| 91106 | ISO/PWI 20186-1 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 1: Isolated cellular RNA | Izstrādē |
| 91107 | ISO/PWI 20186-2 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 2: Isolated genomic DNA | 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 |
| 91108 | ISO/PWI 20186-3 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 3: Isolated circulating cell free DNA from plasma | Izstrādē |
| 87673 | ISO/CD 24051-1.2 | Medical laboratories — Part 1: General principles for the application of artificial intelligence in medical laboratories | Izstrādē |
| 90994 | ISO/WD TS 25646 | In vitro diagnostic medical devices — Definition of analytical performance specifications for laboratory measurements based on medical requirements | Izstrādē |
| 66154 | ISO/WD 35001 | Laboratory biorisk management system — Requirements | Izstrādē |
| 67025 | ISO/PWI 20092 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for blood — Genomic DNA | Izstrādē |
Displaying 131-140 of 142 results.