ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 91103 | ISO/PWI 20166-3 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for formalin-fixed and paraffin-embedded (FFPE) tissue — Part 3: Isolated DNA | Izstrādē |
| 91101 | ISO/PWI 20166-1 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for formalin-fixed and paraffin-embedded (FFPE) tissue — Part 1: Isolated RNA | Izstrādē |
| 26303 | ISO/WD 15191 | Quality assurance, proficiency and accreditation for clinical laboratory medicine | Izstrādē |
| 91108 | ISO/PWI 20186-3 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 3: Isolated circulating cell free DNA from plasma | Izstrādē |
| 91107 | ISO/PWI 20186-2 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 2: Isolated genomic DNA | Izstrādē |
| 91106 | ISO/PWI 20186-1 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 1: Isolated cellular RNA | Izstrādē |
| 91105 | ISO/PWI 20184-2 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for frozen tissue — Part 2: Isolated proteins | Izstrādē |
| 91102 | ISO/PWI 20166-2 | Molecular in vitro diagnostic examinations — Specifications for pre-examinations processes for formalin-fixed and paraffin-embedded (FFPE) tissue — Part 2: Isolated proteins | Izstrādē |
| 69192 | ISO/NP 23640 | In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents | Izstrādē |
| 51983 | ISO/NP 15190 | Medical laboratories — Requirements for safety | Izstrādē |
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