Registration number (WIID)Project No.TitleStatus
37592LVS EN ISO 18113-4:2012In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009)Atcelts
41033LVS CEN/TS 16826-1:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for snap frozen tissue - Part 1: Isolated RNAAtcelts
41046LVS CEN/TS 16827-2:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for FFPE tissue - Part 2: Isolated proteinsAtcelts
5112LVS EN 14254:2004In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humansAtcelts
41041LVS CEN/TS 16835-1:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1: Isolated cellular RNAAtcelts
5067LVS EN 375:1992In vitro diagnostic systems - Requirements for labelling in vitro diagnostic reagents for professional useAtcelts
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
5069EN 928:1995In vitro diagnostic systems - Guidance on the application of EN 29001 and EN 46001 and of EN 29002 and EN 46002 for in vitro diagnostic medical devicesAtcelts
37208LVS EN ISO 16256:2013Clinical laboratory testing and in vitro diagnostic test systems - Reference method for testing the in vitro activity of antimicrobial agents against yeast of fungi involved in infectious diseases (ISO 16256:2012)Atcelts
5073LVS EN 12286:2000 /A1In vitro diagnostic medical devices - Measurement of qiantities in samples of biological origin - Presentation of reference measurement proceduresAtcelts
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