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Key Presentations Announced for Landmark Future of Biosimilars Event Co-Sponsored by DIA and FDLI, Co-Chaired by Merck and PAREXEL
Date:4/28/2011

BOSTON, April 28, 2011 /PRNewswire/ -- PAREXEL International Corporation (NASDAQ: PRXL), a leading global biopharmaceutical services provider, which serves on the Program Committee for "The Future of Biosimilars in the U.S." conference, today announced distinguishing features of this event, which the Drug Information Association (DIA) will host in cooperation with the Food and Drug Law Institute (FDLI).  The landmark event, to be held May 4 - 5, 2011 in Bethesda, Maryland, will feature perspectives of the U.S. Food and Drug Administration (FDA), as well as industry, lawyers, academics, clinicians, payers and patients on the introduction of biosimilars to the U.S.

This first truly comprehensive conference on biosimilars since the enactment of the Biologics Price Competition and Innovation Act (BPCIA) in 2010 will focus on the critical challenges and current ideas of stakeholders impacted by the development and availability of biological medicines in the U.S.  Featured topics will include industry challenges in developing biosimilars and the need for biosimilars, as well as associated economic and legal considerations. The conference program will feature the following key presentations representing patient, regulatory, and industry viewpoints during the first day of the conference, on Wednesday, May 4:

  • Patience Haydock White, M.D., MA, Chief Public Health Officer of the Arthritis Foundation, the nation's largest national, nonprofit health agency working on behalf of 43 million Americans with doctor diagnosed arthritis and related diseases, will present "Patient Access to High Quality, Safe and Effective Biological Medicines" at 8:25 a.m.

  • Steven Kozlowski, M.D., Director, Office of Biotechnology Products, CDER, FDA
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    • SOURCE PAREXEL International Corporation
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