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Europe Biosimilars Rare Diseases

European Commission Continues With Mission To Assess Impact of Orphan Regulation

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Executive Summary

Companies now have a chance to have their say about their experience of EU Orphan Drug Regulation.

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This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

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