ISO/TC 212
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
26310 | ISO/DIS 15198 | Clinical laboratory medicine — In vitro diagnostic medical devices — Validation of manufacturer's recommendations for user quality control | 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 |
90479 | ISO/AWI 25459 | In vitro diagnostic medical devices — Requirements for determining commutability of certified reference materials used as secondary calibrators or trueness controls | Izstrādē |
89155 | ISO/CD 23640 | In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents | Izstrādē |
67024 | ISO/CD 20091 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for blood — Circulating cell free DNA | 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 |
87673 | ISO/CD 24051-1 | Medical laboratories — Part 1: General principles for the application of artificial intelligence in medical laboratories | Izstrādē |
87674 | ISO/AWI 24051-2 | Medical laboratories — Part 2: Digital pathology and artificial intelligence (AI)-based image analysis | Izstrādē |
Displaying 91-100 of 142 results.