ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 26310 | ISO/DIS 15198 | Clinical laboratory medicine — In vitro diagnostic medical devices — Validation of manufacturer's recommendations for user quality control | Izstrādē |
| 85349 | ISO/DIS 18704 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for urine and other body fluids — Isolated cell free DNA | Aptauja slēgta |
| 87738 | ISO/DIS 22367 | Medical laboratories — Application of risk management to medical laboratories | Aptauja |
| 43162 | ISO/DTS 25680 | Medical laboratories - Calculation and expression of measurement uncertainty | Izstrādē |
| 51983 | ISO/NP 15190 | Medical laboratories — Requirements for safety | Izstrādē |
| 69191 | ISO/NP 15197 | In vitro diagnostic test systems — Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus | Izstrādē |
| 67021 | ISO/NP 17822-2 | In vitro diagnostic test systems — Qualitative nucleic acid-based in vitro examination procedures for detection and identification of microbial pathogens — Part 2: Sample preparation and nucleic acid extraction | Izstrādē |
| 69192 | ISO/NP 23640 | In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents | Izstrādē |
| 85074 | ISO/NP TS 17849 | Guidance on the validation and verification of quantitative and qualitative methods | Izstrādē |
| 87549 | ISO/NP TS 22583 | Guidance for supervisors and operators of point-of-care testing (POCT) devices | Izstrādē |
Displaying 81-90 of 142 results.