ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 67027 | ISO/PWI 20094 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for metabolomics in urine, serum and plasma | Izstrādē |
| 67026 | ISO/PWI 20093 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for blood — Cellular RNA | Izstrādē |
| 67025 | ISO/PWI 20092 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for blood — Genomic DNA | Izstrādē |
| 67020 | ISO/PWI 20090 | In vitro diagnostic medical devices — General requirements and definitions for multiplex molecular analysis — Evaluation method of nucleic acid quality | Izstrādē |
| 67018 | ISO/PWI 20089 | Measurement harmonization protocols | Izstrādē |
| 85348 | ISO/PWI 18703 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Isolated circulating cell free RNA from plasma | Izstrādē |
| 67023 | ISO/PWI 17822-4 | In vitro diagnostic test systems — Qualitative nucleic acid-based in vitro examination procedures for detection and identification of microbial pathogens — Part 4: Quality practices for nucleic acid detection and identification | Izstrādē |
| 57706 | ISO/PRF 16782 | Clinical laboratory testing — Criteria for acceptable lots of dehydrated Mueller-Hinton agar and broth for antimicrobial susceptibility testing | Standarts spēkā |
| 87679 | ISO/NP TS 24069 | Medical laboratories — Guidance for personnel competence and development | Izstrādē |
| 87549 | ISO/NP TS 22583 | Guidance for supervisors and operators of point-of-care testing (POCT) devices | Izstrādē |
Displaying 41-50 of 146 results.