ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 67021 | ISO/NP 17822-2 | In vitro diagnostic test systems — Qualitative nucleic acid-based in vitro examination procedures for detection and identification of microbial pathogens — Part 2: Sample preparation and nucleic acid extraction | Izstrādē |
| 69192 | ISO/NP 23640 | In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents | Izstrādē |
| 91317 | ISO/AWI TS 25725 | Design and workflow requirements for NGS-based oncology application | Izstrādē |
| 67216 | ISO/CD 20185 | Molecular in-vitro diagnostic examinations — Specifications for pre-examination processes for blood — Genomic DNA | Izstrādē |
| 51983 | ISO/NP 15190 | Medical laboratories — Requirements for safety | Izstrādē |
| 66154 | ISO/WD 35001 | Laboratory biorisk management system — Requirements | Izstrādē |
| 26302 | ISO/DIS 15190 | Medical laboratories — Requirements for safety | Izstrādē |
| 67029 | ISO/PWI 20096 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for FFPE tissue — RNA | Izstrādē |
| 89155 | ISO/CD 23640 | In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents | Izstrādē |
| 90479 | ISO/AWI 25459 | In vitro diagnostic medical devices — Requirements for determining commutability of certified reference materials used as secondary calibrators or trueness controls | Izstrādē |
Displaying 51-60 of 142 results.