ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 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 |
| 87674 | ISO/CD 24051-2 | Medical laboratories — Part 2: Digital pathology and artificial intelligence (AI)-based image analysis | Izstrādē |
| 31449 | ISO/WD 17593 | Specifications and standards for instruments for self testing in monitoring of anticoagulation treatment | Izstrādē |
| 90121 | ISO/CD 25379-2 | In vitro diagnostic Next Generation Sequencing (NGS) workflows — Part 2: Human RNA examination | Izstrādē |
| 93316 | ISO/AWI 26358 | In vitro diagnostic medical devices — Performance evaluation — Requirements and guidance | Izstrādē |
| 90994 | ISO/CD TS 25646 | In vitro diagnostic medical devices — Definition of analytical performance specifications for laboratory measurements based on medical requirements | Izstrādē |
| 86743 | ISO/AWI TS 20776-3 | ISO/TS 20776-3, Clinical laboratory testing and in vitro diagnostic test systems — Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices — — Part 3: Part 3: Quality performance of disc-diffusion agar method for testing the in vitro activity of antimicrobial agents against rapidly growing aerobic bacteria involved in infectious diseases | Izstrādē |
| 86739 | ISO/CD TS 21385 | Guidance for the implementation of emerging technology in medical laboratories | Izstrādē |
| 93488 | ISO 15195:2018/DAmd 1 | Laboratory medicine — Requirements for the competence of calibration laboratories using reference measurement procedures — Amendment 1 | Izstrādē |
Displaying 121-130 of 146 results.