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[Regulatory aspects of biosimilars. Myths and facts]

C K Schneider1,2,3, M Weise4,5

  • 1Abteilung Arzneimittelzulassung und -Zugänglichkeit, Danish Health and Medicines Authority, Axel Heides Gade 1, 2300, Kopenhagen, Dänemark. ckschneider@gmx.de.

Zeitschrift Fur Rheumatologie
|September 20, 2015
PubMed
Abstract

Keywords:
ApprovalEuropean Medicines AgencyGuidelinesOriginal formulationRegulatory agencies

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