ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 89155 | ISO/CD 23640 | In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents | 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 |
| 87549 | ISO/NP TS 22583 | Guidance for supervisors and operators of point-of-care testing (POCT) devices | Izstrādē |
| 67033 | ISO/PWI 20103 | Clinical performance studies involving specimens from human subjects — Good study practice | Izstrādē |
| 87679 | ISO/PWI TS 24069 | Guidance on personnel training and competence | Izstrādē |
| 87738 | ISO/FDIS 22367 | Medical laboratories — Application of risk management to medical laboratories | Izstrādē |
| 91317 | ISO/AWI TS 25725 | Design and workflow requirements for in vitro diagnostics NGS based oncology application | Izstrādē |
| 88356 | ISO/CD TS 24883 | In Vitro Diagnostic Medical Devices: Lateral Flow Immunoassay for Rapid Diagnostic Testing– General Guidance for Manufacturers | Izstrādē |
| 90120 | ISO/CD 25379-1 | In vitro diagnostic Next Generation Sequencing (NGS) workflows — Part 1: Human DNA examination | Izstrādē |
| 77071 | ISO/PWI 20184-3 | Molecular in vitro diagnostic examinations -- Specifications for pre-examination processes for frozen tissue | Izstrādē |
Displaying 81-90 of 146 results.