ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 87738 | ISO/FDIS 22367 | Medical laboratories — Application of risk management to medical laboratories | Izstrādē |
| 91317 | ISO/AWI TS 25725 | Design and workflow requirements for in vitro diagnostics NGS based oncology application | Izstrādē |
| 88356 | ISO/CD TS 24883 | In Vitro Diagnostic Medical Devices: Lateral Flow Immunoassay for Rapid Diagnostic Testing– General Guidance for Manufacturers | Izstrādē |
| 90479 | ISO/CD 25459 | In vitro diagnostic medical devices — Requirements for determining commutability of certified reference materials used as secondary calibrators or trueness controls | Izstrādē |
| 87674 | ISO/CD 24051-2 | 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 |
| 90121 | ISO/CD 25379-2 | In vitro diagnostic Next Generation Sequencing (NGS) workflows — Part 2: Human RNA examination | Izstrādē |
| 93316 | ISO/PWI 26358 | In vitro diagnostic medical devices — Performance evaluation — Requirements and guidance | Izstrādē |
| 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 |
Displaying 121-130 of 146 results.