ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 90122 | ISO/CD 21474-4 | In vitro diagnostic medical devices — Multiplex molecular testing for nucleic acids — Part 4: Detection of pathogens | Izstrādē |
| 91317 | ISO/WD TS 25725 | Design and workflow requirements for in vitro diagnostics NGS based oncology application | Izstrādē |
| 93491 | ISO/AWI 35001 | Biorisk management for laboratories and other related organisations | Izstrādē |
| 88357 | ISO 24884 | Electronic instructions for use for in vitro diagnostic medical devices — Minimum required information and means of delivery | Izstrādē |
| 88356 | ISO/DTS 24883 | In vitro diagnostic medical devices — General Guidance for manufacturers of lateral flow immunoassay (LFIA) for rapid diagnostic testing (RDT) | Izstrādē |
| 90994 | ISO/CD TS 25646 | In vitro diagnostic medical devices — Definition of analytical performance specifications for laboratory measurements based on medical requirements | Izstrādē |
| 86739 | ISO/DTS 21385 | Recommendations for the implementation of emerging technology in medical laboratories | Izstrādē |
| 91142 | ISO/CD 15197 | In vitro diagnostic test systems — Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus | Izstrādē |
| 91316 | ISO/PWI 25724 | Requirements for open platform polymerase chain reaction (PCR) In Vitro Diagnostic Medical Device (IVD) examinations for tuberculosis diagnosis and antimicrobial susceptibility testing — General Guidance for design, development and manufacture | Izstrādē |
| 67027 | ISO/PWI 20094 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for metabolomics in urine, serum and plasma | Izstrādē |
Displaying 11-20 of 147 results.