ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 91142 | ISO/CD 15197 | In vitro diagnostic test systems — Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus | 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 |
| 67180 | ISO/CD 20167 | Molecular in-vitro diagnostic examinations — Specifications for pre-examination processes for frozen tissue — Extracted proteins | Izstrādē |
| 67216 | ISO/CD 20185 | Molecular in-vitro diagnostic examinations — Specifications for pre-examination processes for blood — Genomic DNA | Izstrādē |
| 93490 | ISO/CD 20776-1 | Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices — Part 1: Broth micro-dilution reference method for testing the in vitro activity of antimicrobial agents against rapidly growing aerobic bacteria involved in infectious diseases | Izstrādē |
| 90122 | ISO/CD 21474-4 | In vitro diagnostic medical devices — Multiplex molecular testing for nucleic acids — Part 4: Detection of pathogens | Izstrādē |
| 87674 | ISO/CD 24051-2.2 | Medical laboratories — Part 2: Digital pathology and artificial intelligence (AI)-based image analysis | Izstrādē |
| 93316 | ISO/CD 26358 | In vitro diagnostic medical devices — Performance evaluation — Requirements and guidance | Izstrādē |
Displaying 71-80 of 147 results.