ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 67033 | ISO/PWI 20103 | Clinical performance studies involving specimens from human subjects — Good study practice | Izstrādē |
| 87679 | ISO/AWI TS 24069 | Medical laboratories — Guidance for personnel competence and development | Izstrādē |
| 34111 | ISO/WD 20259 | In vitro diagnostic medical devices — Labelling and dissemination of product information for in vitro diagnostic products | Izstrādē |
| 91317 | ISO/WD TS 25725 | Design and workflow requirements for in vitro diagnostics NGS based oncology application | Izstrādē |
| 88356 | ISO/DTS 24883 | In vitro diagnostic medical devices — General Guidance for manufacturers of lateral flow immunoassay (LFIA) for rapid diagnostic testing (RDT) | 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 |
| 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 |
| 87674 | ISO/CD 24051-2.2 | Medical laboratories — Part 2: Digital pathology and artificial intelligence (AI)-based image analysis | Izstrādē |
| 93491 | ISO/AWI 35001 | Biorisk management for laboratories and other related organisations | 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 |
Displaying 11-20 of 147 results.