ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 31449 | ISO/WD 17593 | Specifications and standards for instruments for self testing in monitoring of anticoagulation treatment | Izstrādē |
| 67020 | ISO/PWI 20090 | In vitro diagnostic medical devices — General requirements and definitions for multiplex molecular analysis — Evaluation method of nucleic acid quality | Izstrādē |
| 77071 | ISO/PWI 20184-3 | Molecular in vitro diagnostic examinations -- Specifications for pre-examination processes for frozen tissue | Izstrādē |
| 69192 | ISO/NP 23640 | In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents | Izstrādē |
| 90122 | ISO/AWI 21474-4 | In vitro diagnostic medical devices — Multiplex molecular testing for nucleic acids — Part 4: Detection of pathogens | Izstrādē |
| 90121 | ISO/WD 25379-2 | In vitro diagnostic Next Generation Sequencing (NGS) workflows — Part 2: Human RNA examination | Izstrādē |
| 90120 | ISO/WD 25379-1 | In vitro diagnostic Next Generation Sequencing (NGS) workflows — Part 1: Human DNA examination | Izstrādē |
| 91103 | ISO/PWI 20166-3 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for formalin-fixed and paraffin-embedded (FFPE) tissue — Part 3: Isolated DNA | Izstrādē |
| 67033 | ISO/PWI 20103 | Clinical performance studies involving specimens from human subjects — Good study practice | Izstrādē |
| 87549 | ISO/NP TS 22583 | Guidance for supervisors and operators of point-of-care testing (POCT) devices | Izstrādē |
Displaying 41-50 of 142 results.