ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 87680 | ISO/TS 22583:2024 | Requirements and recommendations for supervisors and operators of point-of-care testing (POCT) equipment | Standarts spēkā |
| 87738 | ISO/FDIS 22367 | Medical laboratories — Application of risk management to medical laboratories | Izstrādē |
| 88356 | ISO/CD TS 24883 | Lateral flow immunoassay for rapid diagnostic testing — General guidance for manufacturers | Izstrādē |
| 88357 | ISO/DIS 24884 | Electronic instructions for use for in vitro diagnostic medical devices — Minimum required information and means of delivery | Aptauja |
| 88418 | ISO 35001:2019/Amd 1:2024 | Biorisk management for laboratories and other related organisations — Amendment 1: Climate action changes | Standarts spēkā |
| 89155 | ISO/CD 23640 | In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents | Izstrādē |
| 90120 | ISO/CD 25379-1 | In vitro diagnostic Next Generation Sequencing (NGS) workflows — Part 1: Human DNA examination | 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 |
| 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 |
Displaying 121-130 of 143 results.