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CBI
The Leader in Conferences for the Pharmaceutical Industry
James Class Ph.D.
Michael Castagna
Magdalena Leszczyniecka Ph.D., MBA
Carrie Burke
John M. Pakulski R.Ph.
Julia Hummelt
Sophie Opdyke
Richard Dolinar M.D.
Brian E. Harvey MD, PhD
Rivka Riven Kreitman Ph.D.

CBI’s 7th Summit on Biosimilars and Follow-On Biologics

Analyze the Regulatory Landscape, Market Competition and Clinical Process to Maximize Commercial Potential

March 5-6, 2012
  • Washington, District of Columbia

Position Yourself for Commercial Success in the Evolving Biosimilars Landscape

With the FDA releasing new guidelines concerning the development of biosimilars, understanding the regulatory and commercial realities of the biologics market is more important than ever. Join the discussion as your industry peers address this for the very first time as a group at CBI’s 7th Summit on Biosimilars and Follow-On Biologics.

Our summit places unique focus on the assessment of market access, strategies for effective commercialization and options for interchangeability.  Explore the current climate for biosimilars business including evaluation of the competitive landscape, reimbursement considerations and patient safety. 

This interactive forum covers :

  • Understanding the nuances and implications of the FDA guidelines on biosimilars
  • Analyzing Europe’s role in biosimilar development
  • Determining the appropriate pricing scheme for biosimilars
  • Ensuring appropriate nomenclature and labeling of biosimilars
  • Comparing the challenges of interchangeable vs. similar biologics

 

SEE WHO YOU'LL MEET!