This document gives guidelines on the handling, storage, processing and documentation of humanvenous whole blood specimens intended for the examination of RNA isolated from circulating tumourcells (CTCs) during the pre-examination phase before a molecular examination is performed.This document is applicable to molecular in vitro diagnostic examinations including laboratorydeveloped tests performed by medical laboratories. It is also intended to be used by laboratorycustomers, in vitro diagnostics developers and manufacturers, biobanks, institutions and commercialorganizations performing biomedical research, and regulatory authorities.
Cross References: EN ISO 15189:2012 ISO 15189:2012 EN ISO/IEC 17020 (ISO/IEC 17020:2012) AS ISO/IEC 17020:2012 CEN/TS 17390-3
All current amendments available at time of purchase are included with the purchase of this document.
Product Details
Published: 01/24/2020 ISBN(s): 9780539127041 Number of Pages: 28 File Size: 1 file , 790 KB Product Code(s): 30409967, 30409967, 30409967
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