ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 81712 | ISO/TS 5798:2022 | In vitro diagnostic test systems — Requirements and recommendations for detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) by nucleic acid amplification methods | Atcelts |
| 70960 | ISO 21474-1:2020 | In vitro diagnostic medical devices — Multiplex molecular testing for nucleic acids — Part 1: Terminology and general requirements for nucleic acid quality evaluation | Atcelts |
| 35173 | ISO 22870:2006 | Point-of-care testing (POCT) — Requirements for quality and competence | 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 |
| 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 |
| 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 |
| 67024 | ISO/CD 20091 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for blood — Circulating cell free DNA | Izstrādē |
| 67178 | ISO/CD 20165 | Molecular in-vitro diagnostic examinations — Specifications for pre-examination processes for FFPE tissue — Extracted proteins | Izstrādē |
| 67180 | ISO/CD 20167 | Molecular in-vitro diagnostic examinations — Specifications for pre-examination processes for frozen tissue — Extracted proteins | Izstrādē |
| 67028 | ISO/PWI 20095 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for frozen tissue — RNA | Izstrādē |
Displaying 71-80 of 142 results.