ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 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 |
| 88418 | ISO 35001:2019/Amd 1:2024 | Biorisk management for laboratories and other related organisations — Amendment 1: Climate action changes | 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 |
| 54868 | ISO 23640:2011 | In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents | Standarts spēkā |
| 69445 | ISO/TS 20914:2019 | Medical laboratories — Practical guidance for the estimation of measurement uncertainty | Standarts spēkā |
| 74800 | ISO 23162:2021 | Basic semen examination — Specification and test methods | Standarts spēkā |
| 59944 | ISO/TS 17518:2015 | Medical laboratories — Reagents for staining biological material — Guidance for users | Standarts spēkā |
| 76677 | ISO 15189:2022 | Medical laboratories — Requirements for quality and competence | 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 |
| 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 |
Displaying 1-10 of 142 results.