ISO/TC 212
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
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 |
87549 | ISO/NP TS 22583 | Guidance for supervisors and operators of point-of-care testing (POCT) devices | Izstrādē |
85074 | ISO/NP TS 17849 | Guidance on the validation and verification of quantitative and qualitative methods | Izstrādē |
69192 | ISO/NP 23640 | In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents | Izstrādē |
67021 | ISO/NP 17822-2 | In vitro diagnostic test systems — Qualitative nucleic acid-based in vitro examination procedures for detection and identification of microbial pathogens — Part 2: Sample preparation and nucleic acid extraction | Izstrādē |
69191 | ISO/NP 15197 | In vitro diagnostic test systems — Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus | Izstrādē |
51983 | ISO/NP 15190 | Medical laboratories — Requirements for safety | Izstrādē |
43162 | ISO/DTS 25680 | Medical laboratories - Calculation and expression of measurement uncertainty | Izstrādē |
87738 | ISO/DIS 22367 | Medical laboratories — Application of risk management to medical laboratories | Aptauja |
Displaying 51-60 of 142 results.