Registration number (WIID)Project No.TitleStatus
74322LVS CEN ISO/TS 5798:2023In 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)Standarts spēkā
32667LVS CEN ISO/TS 22367:2010Medical laboratories - Reduction of error through risk management and continual improvement (ISO/TS 22367:2008, including Cor 1:2009)Atcelts
78630FprEN ISO 22367Medical laboratories - Application of risk management to medical laboratories (ISO/FDIS 22637:2026)Izstrādē
73608FprEN ISO 15194In vitro diagnostic medical devices - Requirements for certified reference materials and the content of supporting documentation (ISO/FDIS 15194:2026)Izstrādē
33852FprEN ISO 15193In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for content and presentation of reference measurement procedures (ISO 15193:2009)Izstrādē
73607FprEN ISO 15193In vitro diagnostic medical devices - Requirements for reference measurement procedures (ISO/FDIS 15193:2026)Izstrādē
70518EN ISO 6717:2021In vitro diagnostic medical devices - Single-use containers for the collection of specimens, other than blood, from humans (ISO/DIS 6717:2020)Izstrādē
61692EN ISO 6710:2017Single-use containers for human venous blood specimen collection (ISO 6710:2017)Standarts spēkā
77643EN ISO 5649:2024Medical laboratories - Concepts and specifications for the design, development, implementation, and use of laboratory-developed tests (ISO 5649:2024)Standarts spēkā
72259EN ISO 4307:2021Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for saliva - Isolated human DNA (ISO/DIS 4307:2021)Izstrādē
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