ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 67026 | ISO/PWI 20093 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for blood — Cellular RNA | Izstrādē |
| 67029 | ISO/PWI 20096 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for FFPE tissue — RNA | Izstrādē |
| 85348 | ISO/PWI 18703 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Isolated circulating cell free RNA from plasma | Izstrādē |
| 89155 | ISO/CD 23640 | In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents | Izstrādē |
| 67180 | ISO/CD 20167 | Molecular in-vitro diagnostic examinations — Specifications for pre-examination processes for frozen tissue — Extracted proteins | Izstrādē |
| 85347 | ISO/PWI TS 18702 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for exosomes and other extracellular vesicles in venous whole blood — DNA, RNA and proteins | Izstrādē |
| 71119 | ISO 22870:2016 | Point-of-care testing (POCT) — Requirements for quality and competence | Atcelts |
| 38363 | ISO 15195:2003 | Laboratory medicine — Requirements for reference measurement laboratories | Atcelts |
| 38590 | ISO/TR 18112:2006 | Clinical laboratory testing and in vitro diagnostic test systems — In vitro diagnostic medical devices for professional use — Summary of regulatory requirements for information supplied by the manufacturer | Atcelts |
| 40984 | ISO 18113-1:2009 | In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirements | Atcelts |
Displaying 61-70 of 142 results.