ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 34111 | ISO/WD 20259 | In vitro diagnostic medical devices — Labelling and dissemination of product information for in vitro diagnostic products | Izstrādē |
| 85346 | ISO/PWI TS 18701 | Molecular in vitro diagnostic examinations — Specificationsfor pre-examination processes for human specimens — Isolated microbiome DNA | Izstrādē |
| 87738 | ISO/FDIS 22367 | Medical laboratories — Application of risk management to medical laboratories | Izstrādē |
| 67023 | ISO/PWI 17822-4 | In vitro diagnostic test systems — Qualitative nucleic acid-based in vitro examination procedures for detection and identification of microbial pathogens — Part 4: Quality practices for nucleic acid detection and identification | Izstrādē |
| 67030 | ISO/PWI 20097 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for FFPE tissue — Proteins | Izstrādē |
| 67026 | ISO/PWI 20093 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for blood — Cellular RNA | Izstrādē |
| 91317 | ISO/AWI TS 25725 | Design and workflow requirements for in vitro diagnostics NGS based oncology application | 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 |
| 93488 | ISO 15195:2018/AWI Amd 1 | Laboratory medicine — Requirements for the competence of calibration laboratories using reference measurement procedures — Amendment 1 | Izstrādē |
Displaying 21-30 of 146 results.