CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 81454 | prEN ISO 25379-1 | In vitro diagnostic Next Generation Sequencing (NGS) workflows -- Part 1: Part 1: Human DNA examination | Izstrādē |
| 61687 | EN ISO 20186-2:2019 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2: Isolated genomic DNA (ISO 20186-2:2019) | Izstrādē |
| 61692 | EN ISO 6710:2017 | Single-use containers for human venous blood specimen collection (ISO 6710:2017) | Izstrādē |
| 64279 | EN ISO 22367:2020 | Medical laboratories - Application of risk management to medical laboratories (ISO 22367:2020) | Izstrādē |
| 27341 | EN ISO 15193:2009 | In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for content and presentation of reference measurement procedures (ISO/FDIS 15193:2009) | Izstrādē |
| 74322 | CEN 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 (ISO/TS 5798:2022) | Izstrādē |
| 5109 | EN 13532:2002 | General requirements for in vitro diagnostic medical devices for self-testing | Izstrādē |
| 61690 | EN ISO 20166-2:2018 | Molecular in vitro diagnostic examinations - Specifications for pre-examinations processes for formalin-fixed and paraffin-embedded (FFPE) tissue - Part 2: Isolated proteins (ISO 20166-2:2018) | Izstrādē |
| 29047 | EN 14820:2004/prA1 | Single-use containers for human venous blood specimen collection | Izstrādē |
| 27354 | EN ISO 15194:2009 | In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for certified reference materials and the content of supporting documentation (ISO/FDIS 15194:2009) | Izstrādē |
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