ISO/TC 212
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
67180 | ISO/CD 20167 | Molecular in-vitro diagnostic examinations — Specifications for pre-examination processes for frozen tissue — Extracted proteins | Izstrādē |
67178 | ISO/CD 20165 | Molecular in-vitro diagnostic examinations — Specifications for pre-examination processes for FFPE tissue — Extracted proteins | Izstrādē |
67024 | ISO/CD 20091 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for blood — Circulating cell free DNA | Izstrādē |
26310 | ISO/DIS 15198 | Clinical laboratory medicine — In vitro diagnostic medical devices — Validation of manufacturer's recommendations for user quality control | Izstrādē |
91108 | ISO/PWI 20186-3 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 3: Isolated circulating cell free DNA from plasma | Izstrādē |
69191 | ISO/NP 15197 | In vitro diagnostic test systems — Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus | Izstrādē |
88357 | ISO/CD 24884 | Electronic Instructions for Use for In Vitro Diagnostic Medical Devices (Minimum required information and means of delivery) | Izstrādē |
88356 | ISO/CD TS 24883 | Lateral flow immunoassay for rapid diagnostic testing — General guidance for manufacturers | Izstrādē |
67216 | ISO/CD 20185 | Molecular in-vitro diagnostic examinations — Specifications for pre-examination processes for blood — Genomic DNA | Izstrādē |
91107 | ISO/PWI 20186-2 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 2: Isolated genomic DNA | Izstrādē |
Displaying 131-140 of 142 results.