FDAnews Drug Daily Bulletin
Pharmaceuticals / Commercial Operations

European Commission Publishes Q&A Leaflet on Biosimilars

Jan. 31, 2017
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The European Commission has released a new guide to biosimilars.

The patient-focused document covers topics ranging from the definition of a biosimilar to how biosimilars are integrated in treatment, and includes additional sources for patients to review biosimilar products approved in the European Union.

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