This article addresses some issues involved in meeting regulatory characterization expectations for biosimilars by answering the following questions: What regulatory guidelines are associated with structural characterization and comparability/biosimilarity testing? What complicates the characterization of complex (glyco)protein products? When is analytical characterization required? And which techniques (old and new) are suitable for this application?
Amman, Al-Jbeiha, Yajouz Street,
Caracas Building, Entrance No1, 3rd Floor, Office 311, 11193,
Amman, Jordan