Sandoz gets EU approval for biosimilar epoetin alfa

9 September 2007

Swiss drug major Novartis' generics unit Sandoz has become the first company to develop and receive European Commission approval for its biosimilar epoetin alfa, achieving another important milestone in its efforts to bring high quality, cost-effective biological medicines to patients.

The EC's decision to grant this approval followed a positive opinion in June from the European Medicines Agency's (EMEA) Committee on Medicinal Products for Human Use

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