ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 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 |
| 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 |
| 69801 | ISO 20184-2:2018 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for frozen tissue — Part 2: Isolated proteins | Standarts spēkā |
| 81506 | ISO 5649:2024 | Medical laboratories — Concepts and specifications for the design, development, implementation and use of laboratory-developed tests | Standarts spēkā |
| 71293 | ISO 35001:2019 | Biorisk management for laboratories and other related organisations | Standarts spēkā |
| 78024 | ISO 21474-2:2022 | In vitro diagnostic medical devices — Multiplex molecular testing for nucleic acids — Part 2: Validation and verification | 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 |
| 59944 | ISO/TS 17518:2015 | Medical laboratories — Reagents for staining biological material — Guidance for users | Standarts spēkā |
| 83565 | ISO 21474-3:2024 | In vitro diagnostic medical devices — Multiplex molecular testing for nucleic acids — Part 3: Interpretation and reports | Standarts spēkā |
| 42021 | ISO 15193:2009 | In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Requirements for content and presentation of reference measurement procedures | Standarts spēkā |
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