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
65451CEN/TS 17390-3:2020Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood - Part 3: Preparations for analytical CTC stainingAtcelts
41046CEN/TS 16827-2:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for FFPE tissue - Part 2: Isolated proteinsAtcelts
27618EN ISO 18113-3:2009In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO/FDIS 18113-3:2009)Atcelts
41047CEN/TS 16826-2:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for snap frozen tissue - Part 2: Isolated proteinsAtcelts
41041CEN/TS 16835-1:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1: Isolated cellular RNAAtcelts
41045CEN/TS 16835-2:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2: Isolated genomic DNAAtcelts
27616EN ISO 18113-1:2009In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO/FDIS 18113-1:2009)Atcelts
41044CEN/TS 16827-3:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for FFPE tissue - Part 3: Isolated DNAAtcelts
64279EN ISO 22367:2020Medical laboratories - Application of risk management to medical laboratories (ISO 22367:2020)Atcelts
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