ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 87673 | ISO/DIS 24051-1 | Medical laboratories — Part 1: General principles for the application of artificial intelligence in medical laboratories | Aptauja |
| 88357 | ISO/DIS 24884 | Electronic instructions for use for in vitro diagnostic medical devices — Minimum required information and means of delivery | Aptauja slēgta |
| 78110 | ISO 20184-3:2021 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for frozen tissue — Part 3: Isolated DNA | Standarts spēkā |
| 69803 | ISO 20166-3:2018 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for formalin-fixed and paraffin-embedded (FFPE) tissue — Part 3: Isolated DNA | Standarts spēkā |
| 74800 | ISO 23162:2021 | Basic semen examination — Specification and test methods | Standarts spēkā |
| 71254 | ISO 22367:2020 | Medical laboratories — Application of risk management to medical laboratories | Standarts spēkā |
| 84816 | ISO/TS 16766:2024 | Manufacturers’ considerations for in vitro diagnostic medical devices in a public health emergency | Standarts spēkā |
| 75442 | ISO 20166-4:2021 | Molecular in vitro diagnostic examinations — Specifications for preexamination processes for formalin-fixed and paraffin-embedded (FFPE) tissue — Part 4: In situ detection techniques | Standarts spēkā |
| 54868 | ISO 23640:2011 | In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents | Standarts spēkā |
| 72141 | ISO/TS 16782:2016 | Clinical laboratory testing — Criteria for acceptable lots of dehydrated Mueller-Hinton agar and broth for antimicrobial susceptibility testing | Standarts spēkā |
Displaying 101-110 of 146 results.