Registration number (WIID)Project No.TitleStatus
41041LVS CEN/TS 16835-1:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1: Isolated cellular RNAAtcelts
37592EN ISO 18113-4:2011In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009)Atcelts
65450CEN/TS 17390-1:2020Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood - Part 1: Isolated RNAAtcelts
5094EN 591:1994In vitro diagnostic systems - Requirements for user manuals for in vitro diagnostic instruments for professional useAtcelts
24452EN ISO 22870:2006Point-of-care testing (POCT) - Requirements for quality and competence (ISO 22870:2006)Atcelts
37591EN ISO 18113-3:2011In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009)Atcelts
32667CEN ISO/TS 22367:2010Medical laboratories - Reduction of error through risk management and continual improvement (ISO/TS 22367:2008, including Cor 1:2009)Atcelts
5067LVS EN 375:1992In vitro diagnostic systems - Requirements for labelling in vitro diagnostic reagents for professional useAtcelts
5075EN 829:1996In vitro diagnostic systems - Transport packages for medical and biological specimens - Requirements, testsAtcelts
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
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