Recommendations for in vitro evaluation of blood components collected, prepared and stored in non‐<scp>DEHP</scp> medical devices

Abstract

Studies in the scope of evaluating the quality of blood products obtained with non-DEHP devices, under the condition that they are carried out according to these recommendations, could be used by all members of the EBA to serve as scientific support in the authorization process specific to their jurisdiction or for their internal validation use.