ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 77071 | ISO/PWI 20184-3 | Molecular in vitro diagnostic examinations -- Specifications for pre-examination processes for frozen tissue | Izstrādē |
| 90120 | ISO/CD 25379-1 | In vitro diagnostic Next Generation Sequencing (NGS) workflows — Part 1: Human DNA examination | Izstrādē |
| 26307 | ISO/DIS 15195 | Clinical laboratory medicine — Requirements for reference measurement laboratories | Izstrādē |
| 43162 | ISO/DTS 25680 | Medical laboratories - Calculation and expression of measurement uncertainty | Izstrādē |
| 39737 | ISO/WD 20776 | Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility devices | Izstrādē |
| 26308 | ISO/CD 15196 | Identification and determination of analytical and clinical performance goals for laboratory methodologies | Izstrādē |
| 26311 | ISO/WD 15199 | Symbols used in labelling of in vitro diagnostic products | Izstrādē |
| 50761 | ISO/WD 11764 | Clinical laboratory testing — Susceptibility testing of fungi | Izstrādē |
| 67020 | ISO/PWI 20090 | In vitro diagnostic medical devices — General requirements and definitions for multiplex molecular analysis — Evaluation method of nucleic acid quality | Izstrādē |
| 85074 | ISO/AWI TS 17849 | Guidance on the validation and verification of quantitative and qualitative methods | Izstrādē |
Displaying 101-110 of 146 results.
