Registration number (WIID)Project No.TitleStatus
29869prEN 13532General requirements for in vitro diagnostic medical devices for self-testingIzstrādē
5090EN 1659:1996In vitro diagnostic systems - Culture media for microbiology - Terms and definitionsIzstrādē
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
25090prEN ISO 15194In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Description of reference materialsIzstrādē
29673prEN ISO 15190Medical laboratories - Requirements for safetyIzstrādē
73608FprEN ISO 15194In vitro diagnostic medical devices - Requirements for certified reference materials and the content of supporting documentation (ISO/FDIS 15194:2026)Izstrādē
25658EN ISO 15189:2003/prA1Medical laboratories - Particular requirements for quality and competence - Amendment 1 (ISO 15189:2003/DAM 1:2005)Izstrādē
25229prCEN ISO/TS 22367Medical laboratories - Reduction of error through risk management and continual improvementIzstrādē
61691EN ISO 20166-3:2019Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for formalin-fixed and paraffin-embedded (FFPE) tissue - Part 3: Isolated DNA (ISO/DIS 20166-3:2016)Izstrādē
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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