Registration number (WIID)Project No.TitleStatus
29868prEN 13641Elimination or reduction of risk of infection related to in vitro diagnostic reagentsIzstrādē
29673prEN ISO 15190Medical laboratories - Requirements for safetyIzstrādē
25229prCEN ISO/TS 22367Medical laboratories - Reduction of error through risk management and continual improvementIzstrādē
77417prCEN ISO/TS 18702Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for exosomes and other extracellular vesicles in venous whole blood - DNA, RNA and proteinsIzstrādē
68066EN ISO 23118:2021Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma (ISO/DIS 23118:2020)Izstrādē
31365EN ISO 19001:2013In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology (ISO/DIS 19001:2010)Izstrādē
60920prEN ISO 15197 revIn vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitusIzstrādē
81156prEN ISO 15197 revIn vitro diagnostic test systems — Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitusIzstrādē
67446CEN/TS 17626:2021Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for human specimen - Isolated microbiome DNAIzstrādē
73607FprEN ISO 15193In vitro diagnostic medical devices - Requirements for reference measurement procedures (ISO/FDIS 15193:2026)Izstrādē
Displaying 221-230 of 277 results.