ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 90120 | ISO/DIS 25379-1 | In vitro diagnostic Next Generation Sequencing (NGS) workflows — Part 1: Human DNA examination | Izstrādē |
| 89155 | ISO/DIS 23640 | In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents | Aptauja slēgta |
| 88418 | ISO 35001:2019/Amd 1:2024 | Biorisk management for laboratories and other related organisations — Amendment 1: Climate action changes | Standarts spēkā |
| 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 |
| 87738 | ISO 22367:2026 | Medical laboratories — Application of risk management to medical laboratories | Standarts spēkā |
| 87680 | ISO/TS 22583:2024 | Requirements and recommendations for supervisors and operators of point-of-care testing (POCT) equipment | Standarts spēkā |
| 87679 | ISO/AWI TS 24069 | Medical laboratories — Guidance for personnel competence and development | Izstrādē |
| 87674 | ISO/CD 24051-2.2 | Medical laboratories — Part 2: Digital pathology and artificial intelligence (AI)-based image analysis | Izstrādē |
| 87673 | ISO/DIS 24051-1 | Medical laboratories — Part 1: General principles for the application of artificial intelligence in medical laboratories | Aptauja slēgta |
Displaying 21-30 of 147 results.