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Biosimilar Rules Evolve in Europe

EMA Seeks Industry Comments On IFN-Beta Draft Guideline

By Nuala Moran
BioWorld International Correspondent

Wednesday, January 25, 2012
LONDON – Pressing on with its mission of establishing regulatory pathways for more complex biosimilar drugs, the European Medicines Agency (EMA) published a draft guideline on a proposed route for approving interferon beta (IFN-beta) for treating multiple sclerosis.

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