ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 26302 | ISO/DIS 15190 | Medical laboratories — Requirements for safety | Izstrādē |
| 67029 | ISO/PWI 20096 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for FFPE tissue — RNA | Izstrādē |
| 67028 | ISO/PWI 20095 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for frozen tissue — RNA | Izstrādē |
| 90121 | ISO/CD 25379-2 | In vitro diagnostic Next Generation Sequencing (NGS) workflows — Part 2: Human RNA examination | 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 | Medical laboratories — Part 2: Digital pathology and artificial intelligence (AI)-based image analysis | Izstrādē |
| 93316 | ISO/AWI 26358 | In vitro diagnostic medical devices — Performance evaluation — Requirements and guidance | 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 |
| 77071 | ISO/PWI 20184-3 | Molecular in vitro diagnostic examinations -- Specifications for pre-examination processes for frozen tissue | Izstrādē |
| 88356 | ISO/CD TS 24883 | In Vitro Diagnostic Medical Devices: Lateral Flow Immunoassay for Rapid Diagnostic Testing– General Guidance for Manufacturers | Izstrādē |
Displaying 131-140 of 146 results.