ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 35172 | ISO/TR 22869:2005 | Medical laboratories Guidance on laboratory implementation of ISO 15189: 2003 | Atcelts |
| 35172 | ISO/TR 22869:2005 | Medical laboratories — Guidance on laboratory implementation of ISO 15189: 2003 | Atcelts |
| 38590 | ISO/TR 18112:2006 | Clinical laboratory testing and in vitro diagnostic test systems — In vitro diagnostic medical devices for professional use — Summary of regulatory requirements for information supplied by the manufacturer | Atcelts |
| 87679 | ISO/PWI TS 24069 | Guidance on personnel training and competence | Izstrādē |
| 85347 | ISO/PWI TS 18702 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for exosomes and other extracellular vesicles in venous whole blood — DNA, RNA and proteins | Izstrādē |
| 85346 | ISO/PWI TS 18701 | Molecular in vitro diagnostic examinations — Specificationsfor pre-examination processes for human specimens — Isolated microbiome DNA | Izstrādē |
| 93316 | ISO/PWI 26358 | In vitro diagnostic medical devices – Performance evaluation – Requirements and guidance | 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 |
| 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 |
Displaying 21-30 of 143 results.