Biosimilars – Understanding the Regulatory Challenges

July 16, 2013 8:58 AM

Center for Professional Innovation and Education, Inc. is organizing the Biosimilars – Understanding the Regulatory Challenges in King of Prussia, Pennsylvania on 4-5 November 2013.

Why this conference?
To better understand what the developing FDA biosimilar pathway might look like, this course will closely examine the existing regulatory guidelines from the European Medicine Agency (EMA) and the World Health Organization (WHO), and compare them to the draft FDA guidances. Insights and practical suggestions to help your company enter the biosimilar biological product market will be provided by examining what has worked, and what has not, for the existing market-approved EMA biosimilars and FDA follow-on-proteins.

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