Registration number (WIID)Project No.TitleStatus
76940LVS CEN ISO/TS 7552-2:2024Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumour cells (CTCs) in venous whole blood - Part 2: Isolated DNA (ISO/TS 7552-2:2024)Standarts spēkā
68157EN ISO 15189:2022Medical laboratories - Requirements for quality and competence (ISO/DIS 15189:2021)Standarts spēkā
79016EN ISO 15189:2022/A11:2023Medical laboratories - Requirements for quality and competenceStandarts spēkā
61692EN ISO 6710:2017Single-use containers for human venous blood specimen collection (ISO 6710:2017)Standarts spēkā
75465CEN/TS 17981-2:2023In vitro diagnostic Next Generation Sequencing (NGS) workflows - Part 2: Human RNA examinationStandarts spēkā
70932EN ISO 18113-4:2024In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2022)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
61692LVS EN ISO 6710:2017Single-use containers for human venous blood specimen collection (ISO 6710:2017)Standarts spēkā
77454EN ISO 18704:2026Molecular in vitro diagnostic examinations - Requirements and recommendations for pre-examination processes for urine and other body fluids - Isolated cell-free DNA (ISO 18704:2026)Standarts spēkā
68157LVS EN ISO 15189:2023Medical laboratories - Requirements for quality and competence (ISO 15189:2022)Standarts spēkā
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