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Biosimilars Industry Celebrates EMA’s Plan to Reduce Clinical Trials

Paper On Streamlining Development Wins Plaudits At Medicines for Europe Conference

 
• By Dave Wallace

The European Medicines Agency’s latest move towards a more streamlined process for biosimilar registration in Europe was the hottest topic at last week’s annual biosimilars conference held by Medicines for Europe in Amsterdam.

Biosimilars are heading for a more streamlined path to market in Europe (Shutterstock)

The European Medicines Agency’s publication of a draft reflection paper on a tailored clinical approach for biosimilar development is “exciting news” that “represents the next step in this journey to enable streamlined biosimilar development in the EU.”

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