ISO/TC 212
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
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 |
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 |
87679 | ISO/PWI TS 24069 | Guidance on personnel training and competence | Izstrādē |
91317 | ISO/AWI TS 25725 | Design and workflow requirements for NGS-based oncology application | Izstrādē |
90994 | ISO/AWI TS 25646 | In vitro diagnostic medical devices — Definition of analytical performance specifications for laboratory measurements based on medical requirements | Izstrādē |
Displaying 81-90 of 142 results.