ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 69192 | ISO/NP 23640 | In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents | Izstrādē |
| 51983 | ISO/NP 15190 | Medical laboratories — Requirements for safety | 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 |
| 67028 | ISO/PWI 20095 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for frozen tissue — RNA | Izstrādē |
| 67180 | ISO/CD 20167 | Molecular in-vitro diagnostic examinations — Specifications for pre-examination processes for frozen tissue — Extracted proteins | Izstrādē |
| 67178 | ISO/CD 20165 | Molecular in-vitro diagnostic examinations — Specifications for pre-examination processes for FFPE tissue — Extracted proteins | Izstrādē |
| 67024 | ISO/CD 20091 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for blood — Circulating cell free DNA | Izstrādē |
| 26310 | ISO/DIS 15198 | Clinical laboratory medicine — In vitro diagnostic medical devices — Validation of manufacturer's recommendations for user quality control | Izstrādē |
| 91317 | ISO/AWI TS 25725 | Design and workflow requirements for NGS-based oncology application | Izstrādē |
Displaying 101-110 of 142 results.