CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 64279 | EN ISO 22367:2020 | Medical laboratories - Application of risk management to medical laboratories (ISO/DIS 22367:2019) | Izstrādē |
| 70517 | EN ISO 20184-3:2021 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for frozen tissue - Part 3: Isolated DNA (ISO/DIS 20184-3:2020) | Izstrādē |
| 81454 | prEN ISO 25379-1 | In vitro diagnostic Next Generation Sequencing (NGS) workflows -- Part 1: Part 1: Human DNA examination | Izstrādē |
| 67447 | CEN/TS 17688-1:2021 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for Fine Needle Aspirates (FNAs) - Part 1: Isolated cellular RNA | 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 |
| 64589 | - | Molecular in vitro diagnostic examinations - Specifications for preexamination processes for saliva - Isolated DNA | Izstrādē |
| 5089 | - | Methods for the determination of performance of culture media | Izstrādē |
| 5109 | EN 13532:2002 | General requirements for in vitro diagnostic medical devices for self-testing | Izstrādē |
| 68066 | EN ISO 23118:2021 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma (ISO/DIS 23118:2020) | Izstrādē |
| 31365 | EN ISO 19001:2013 | In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology (ISO/DIS 19001:2010) | Izstrādē |
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