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 |
| 67022 | ISO 17822:2020 | In vitro diagnostic test systems — Nucleic acid amplification-based examination procedures for detection and identification of microbial pathogens — Laboratory quality practice guide | Standarts spēkā |
| 88418 | ISO 35001:2019/Amd 1:2024 | Biorisk management for laboratories and other related organisations — Amendment 1: Climate action changes | Standarts spēkā |
| 74800 | ISO 23162:2021 | Basic semen examination — Specification and test methods | Standarts spēkā |
| 77070 | ISO/TS 23824:2024 | Medical laboratories — Guidance on application of ISO 15189 in anatomic pathology | Standarts spēkā |
| 54868 | ISO 23640:2011 | In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents | Standarts spēkā |
| 51984 | ISO 19001:2013 | In vitro diagnostic medical devices — Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology | Standarts spēkā |
| 72191 | ISO 15190:2020 | Medical laboratories — Requirements for safety | Standarts spēkā |
| 42022 | ISO 15194:2009 | In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Requirements for certified reference materials and the content of supporting documentation | Standarts spēkā |
| 74605 | ISO 23118:2021 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma | Standarts spēkā |
Displaying 131-140 of 142 results.