ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 90994 | ISO/WD TS 25646 | In vitro diagnostic medical devices — Definition of analytical performance specifications for laboratory measurements based on medical requirements | Izstrādē |
| 86739 | ISO/WD TS 21385 | Guidance for emerging technologies intended for medical laboratory use | Izstrādē |
| 66154 | ISO/WD 35001 | Laboratory biorisk management system — Requirements | Izstrādē |
| 39737 | ISO/WD 20776 | Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility devices | Izstrādē |
| 34111 | ISO/WD 20259 | In vitro diagnostic medical devices — Labelling and dissemination of product information for in vitro diagnostic products | Izstrādē |
| 31449 | ISO/WD 17593 | Specifications and standards for instruments for self testing in monitoring of anticoagulation treatment | Izstrādē |
| 26311 | ISO/WD 15199 | Symbols used in labelling of in vitro diagnostic products | Izstrādē |
| 26303 | ISO/WD 15191 | Quality assurance, proficiency and accreditation for clinical laboratory medicine | Izstrādē |
| 50761 | ISO/WD 11764 | Clinical laboratory testing — Susceptibility testing of fungi | Izstrādē |
| 81712 | ISO/TS 5798:2022 | In vitro diagnostic test systems — Requirements and recommendations for detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) by nucleic acid amplification methods | Standarts spēkā |
Displaying 1-10 of 143 results.