ISO/TC 212
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
42640 | ISO 15189:2003/DAmd 1 | Medical laboratories — Particular requirements for quality and competence — Amendment 1 | Izstrādē |
67027 | ISO/PWI 20094 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for metabolomics in urine, serum and plasma | Izstrādē |
88356 | ISO/CD TS 24883 | Lateral flow immunoassay for rapid diagnostic testing — General guidance for manufacturers | 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 |
52820 | ISO 15195:2003/NP Amd 1 | Laboratory medicine — Requirements for reference measurement laboratories — Amendment 1 | Izstrādē |
67177 | ISO/CD 20164 | Molecular in-vitro diagnostic examinations — Specifications for pre-examination processes for FFPE tissue — DNA | Izstrādē |
91316 | ISO/PWI 25724 | Requirements for open platform polymerase chain reaction (PCR) In Vitro Diagnostic Medical Device (IVD) examinations for tuberculosis diagnosis and antimicrobial susceptibility testing – General Guidance for design, development and manufacture | Izstrādē |
67029 | ISO/PWI 20096 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for FFPE tissue — RNA | Izstrādē |
67032 | ISO/PWI 20102 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for frozen tissue — Proteins | Izstrādē |
90120 | ISO/WD 25379-1 | In vitro diagnostic Next Generation Sequencing (NGS) workflows — Part 1: Human DNA examination | Izstrādē |
Displaying 31-40 of 142 results.