ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 81506 | ISO 5649:2024 | Medical laboratories — Concepts and specifications for the design, development, implementation and use of laboratory-developed tests | Standarts spēkā |
| 91142 | ISO/AWI 15197 | In vitro diagnostic test systems — Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus | Izstrādē |
| 90122 | ISO/AWI 21474-4 | In vitro diagnostic medical devices — Multiplex molecular testing for nucleic acids — Part 4: Detection of pathogens | Izstrādē |
| 90479 | ISO/AWI 25459 | In vitro diagnostic medical devices — Requirements for determining commutability of certified reference materials used as secondary calibrators or trueness controls | Izstrādē |
| 90994 | ISO/AWI TS 25646 | In vitro diagnostic medical devices — Definition of analytical performance specifications for laboratory measurements based on medical requirements | Izstrādē |
| 91317 | ISO/AWI TS 25725 | Design and workflow requirements for NGS-based oncology application | Izstrādē |
| 26308 | ISO/CD 15196 | Identification and determination of analytical and clinical performance goals for laboratory methodologies | Izstrādē |
| 67024 | ISO/CD 20091 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for blood — Circulating cell free DNA | Izstrādē |
| 67177 | ISO/CD 20164 | Molecular in-vitro diagnostic examinations — Specifications for pre-examination processes for FFPE tissue — DNA | Izstrādē |
| 67178 | ISO/CD 20165 | Molecular in-vitro diagnostic examinations — Specifications for pre-examination processes for FFPE tissue — Extracted proteins | Izstrādē |
Displaying 61-70 of 142 results.