ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 91317 | ISO/AWI TS 25725 | Design and workflow requirements for NGS-based oncology application | Izstrādē |
| 88356 | ISO/CD TS 24883 | Lateral flow immunoassay for rapid diagnostic testing — General guidance for manufacturers | Izstrādē |
| 89155 | ISO/CD 23640 | In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents | Izstrādē |
| 67030 | ISO/PWI 20097 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for FFPE tissue — Proteins | Izstrādē |
| 90994 | ISO/AWI 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 |
| 67027 | ISO/PWI 20094 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for metabolomics in urine, serum and plasma | Izstrādē |
| 91101 | ISO/PWI 20166-1 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for formalin-fixed and paraffin-embedded (FFPE) tissue — Part 1: Isolated RNA | Izstrādē |
| 31449 | ISO/WD 17593 | Specifications and standards for instruments for self testing in monitoring of anticoagulation treatment | Izstrādē |
Displaying 21-30 of 142 results.