ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 86743 | ISO/AWI TS 20776-3 | ISO/TS 20776-3, Clinical laboratory testing and in vitro diagnostic test systems — Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices — — Part 3: Part 3: Quality performance of disc-diffusion agar method for testing the in vitro activity of antimicrobial agents against rapidly growing aerobic bacteria involved in infectious diseases | Izstrādē |
| 86739 | ISO/DTS 21385 | Recommendations for the implementation of emerging technology in medical laboratories | 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 |
| 43162 | ISO/DTS 25680 | Medical laboratories - Calculation and expression of measurement uncertainty | Izstrādē |
| 91142 | ISO/CD 15197 | In vitro diagnostic test systems — Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus | Izstrādē |
| 83899 | ISO/CD TS 8219 | Requirements for the identification and characterisation of microbes using next generation sequencing direct from clinical specimens in the management of infectious disease | Izstrādē |
| 67026 | ISO/PWI 20093 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for blood — Cellular RNA | Izstrādē |
| 93491 | ISO/AWI 35001 | Biorisk management for laboratories and other related organisations | Izstrādē |
| 26308 | ISO/CD 15196 | Identification and determination of analytical and clinical performance goals for laboratory methodologies | 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 41-50 of 147 results.