ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 89155 | ISO/CD 23640 | In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents | Izstrādē |
| 26303 | ISO/WD 15191 | Quality assurance, proficiency and accreditation for clinical laboratory medicine | Izstrādē |
| 34111 | ISO/WD 20259 | In vitro diagnostic medical devices — Labelling and dissemination of product information for in vitro diagnostic products | Izstrādē |
| 67177 | ISO/CD 20164 | Molecular in-vitro diagnostic examinations — Specifications for pre-examination processes for FFPE tissue — DNA | 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 |
| 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 |
| 56027 | ISO 16256:2012 | Clinical laboratory testing and in vitro diagnostic test systems — Reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infectious diseases | Atcelts |
| 42641 | ISO 15189:2007 | Medical laboratories — Particular requirements for quality and competence | Atcelts |
| 69984 | ISO 17511:2020 | In vitro diagnostic medical devices — Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples | 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 |
Displaying 61-70 of 142 results.