ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 57706 | ISO/PRF 16782 | Clinical laboratory testing — Criteria for acceptable lots of dehydrated Mueller-Hinton agar and broth for antimicrobial susceptibility testing | Standarts spēkā |
| 74800 | ISO 23162:2021 | Basic semen examination — Specification and test methods | Standarts spēkā |
| 70960 | ISO 21474-1:2020 | In vitro diagnostic medical devices — Multiplex molecular testing for nucleic acids — Part 1: Terminology and general requirements for nucleic acid quality evaluation | Standarts spēkā |
| 81506 | ISO 5649:2024 | Medical laboratories — Concepts and specifications for the design, development, implementation and use of laboratory-developed tests | 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 |
| 87738 | ISO 22367:2026 | Medical laboratories — Application of risk management to medical laboratories | Standarts spēkā |
| 76677 | ISO 15189:2022 | Medical laboratories — Requirements for quality and competence | Standarts spēkā |
| 84816 | ISO/TS 16766:2024 | Manufacturers’ considerations for in vitro diagnostic medical devices in a public health emergency | Standarts spēkā |
| 69445 | ISO/TS 20914:2019 | Medical laboratories — Practical guidance for the estimation of measurement uncertainty | Standarts spēkā |
| 67217 | ISO 20186-1:2019 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 1: Isolated cellular RNA | Standarts spēkā |
Displaying 31-40 of 146 results.