home   genetic news   bioinformatics   biotechnology   literature   journals   ethics   positions   events   sitemap
 
  HUM-MOLGEN -> Events -> Meetings and Conferences  
 

The Future of Biosimilars in the US: Legal, Regulatory, Scientific, Regulatory, Clinical and Payer Issues

 
  February 18, 2011  
     
 
Bethesda North Marriott Hotel & Conference Center, Bethesda, MD USA
May 4 2011 8:00AM - May 5 2011 5:00PM


The First Truly Comprehensive Conference on Biosimilars Since the Enactment of BPCIA in 2010.

On March 23, 2010, the Biologics Price Competition and Innovation Act was enacted into law as part of U.S. healthcare reform, establishing an approval pathway for biosimilar biological productsin the US. This Act and the way it is implemented will have huge impact on the development and availability of biological medicines in the US, both from an intellectual property and market access perspective. Hear the perspectives of FDA, industry, lawyers, academics, clinicians, payers and patients on the introduction of biosimilars to the US, including the critical challenges and the current ideas of these stakeholders.

 

Event Code:
11012

 

 
 
Organized by: DIA
Invited Speakers: See website for speaker information
 
Deadline for Abstracts: Call contact
 
Registration:

Joanne Wallace, Program Manager

Phone +1.215.442.6180 

Fax +1.215.442.6199

email Joanne.Wallace@diahome.org

E-mail: joanne.wallace@diahome.org
 
   
 
home   genetic news   bioinformatics   biotechnology   literature   journals   ethics   positions   events   sitemap
 
 
 

Generated by meetings and positions 5.0 by Kai Garlipp
WWW: Kai Garlipp, Frank S. Zollmann.
7.0 © 1995- HUM-MOLGEN. All rights reserved. Liability, Copyright and Imprint.