Separation of Recombinant Human Erythropoietin (rhEPO) using the European Pharmacopoeia Method on the PA 800 plus Pharmaceutical Analysis System

This application note provides guidance for the preparation of an EPO suitability standard and separation buffer. Instrument configuration and set up of the EuPh method parameters for the analysis of EPO in 32 Karat software using the PA 800 plus Pharmaceutical Analysis System are also described.