Registration number (WIID)Project No.TitleStatus
5074EN 12287:1999In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Description of reference materialsAtcelts
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
41042CEN/TS 16827-1:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for FFPE tissue - Part 1: Isolated RNAAtcelts
64279LVS EN ISO 22367:2020Medical laboratories - Application of risk management to medical laboratories (ISO 22367:2020)Atcelts
5115LVS EN 12286:1998/A1:2000In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Presentation of reference measurement proceduresAtcelts
41046CEN/TS 16827-2:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for FFPE tissue - Part 2: Isolated proteinsAtcelts
41045LVS CEN/TS 16835-2:2016Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2: Isolated genomic DNAAtcelts
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
5068EN 376:1992In vitro diagnostic systems - Requirements for labelling in vitro diagnostic reagents for self-testingAtcelts
41040LVS CEN/TS 16835-3:2016Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 3: Isolated circulating cell free DNA from plasmaAtcelts
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