ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 89155 | ISO/DIS 23640 | In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents | Aptauja slēgta |
| 26310 | ISO/DIS 15198 | Clinical laboratory medicine — In vitro diagnostic medical devices — Validation of manufacturer's recommendations for user quality control | Izstrādē |
| 26307 | ISO/DIS 15195 | Clinical laboratory medicine — Requirements for reference measurement laboratories | Izstrādē |
| 26302 | ISO/DIS 15190 | Medical laboratories — Requirements for safety | 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 |
| 90994 | ISO/CD TS 25646 | In vitro diagnostic medical devices — Definition of analytical performance specifications for laboratory measurements based on medical requirements | Izstrādē |
| 93489 | ISO/CD TS 16782 | Clinical laboratory testing — Criteria for acceptable lots of dehydrated Mueller-Hinton agar and broth for antimicrobial susceptibility testing | Izstrādē |
| 93316 | ISO/CD 26358 | In vitro diagnostic medical devices — Performance evaluation — Requirements and guidance | Izstrādē |
| 87674 | ISO/CD 24051-2.2 | Medical laboratories — Part 2: Digital pathology and artificial intelligence (AI)-based image analysis | Izstrādē |
| 90122 | ISO/CD 21474-4 | In vitro diagnostic medical devices — Multiplex molecular testing for nucleic acids — Part 4: Detection of pathogens | Izstrādē |
Displaying 61-70 of 147 results.