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Orphan Drugs Research and Commercialization Conference

 
  December 17, 2012  
     
 
GTCbio, Boston, MA
2013-05-08 to 213-5-10


 GTC is proud to announce its inaugural Orphan Drugs Research and Commercialization Conference at a crucial time in the rare disease space. With new therapies emerging in rare disease treatment and exciting partnerships being forged between big pharma and smaller niche companies, it is clear that the field of rare disease and orphan drug is growing. Rather than merely reciting the challenges of orphan drug development, it is time all stakeholders in the community come together to find innovative solutions in order to better serve rare disease patients.

 

This meeting connects industry, academia, regulators, and patient groups to dialogue about strategies to improve orphan drug research, pricing, reimbursement, access, and other key topics. 

The Orphan Drugs Research and Commercialization Conference is one of four parallel tracks to the 2nd Novel Technologies in Drug Discovery Summit on May 8 - 10,  2013 in Boston, MA. 

Tentative Sessions Include:

Pre-Conference Workshop: Developing an Effective Pricing and Reimbursement Strategy
Novel Therapeutics in Rare Diseases
Designing Effective Clinical Trials Case Studies in the Preclinical and Clinical Space
Partnering in Rare Diseases
Commercialization of Orphan Drugs
Panel Discussion: Regulatory in Orphan Drug Development

 
 
Organized by: GTCbio
Invited Speakers:
Monica Coenraads
Co-Founder & Executive Director 
Rett Syndrome Research Trust
 
Tim Coté
Professor of Practice, Regulatory Affairs 
Keck Graduate Institute
 
Gerry Cox
Vice President of Clinical Development, Rare Diseases Group
Genzyme
 
Christopher A. French
Assistant Professor, Pathology
Harvard Medical School and Brigham and Women's Hospital
 
Pat Furlong
 
Founding President & CEO
 Parent Project Muscular Dystrophy
 
Cláudia Hirawat
Senior Vice President, Corporate Development
PTC Therapeutics
 
Nicolas Koebel
Global Commercial Lead, Rare Diseases
GlaxoSmithKline
 
Fulvio Mavilio
Chief Scientific Officer
Genethon
 
Ramaiah Muthyala
Associate Director, Center for Orphan Drug Development
University of Minnesota
 
May Orfali
Senior Director, Rare Diseases Department
Pfizer
 
Stephanie Okey
Vice President & General Manager, Rare Diseases, U.S Genetic Diseases
Genzyme
 
Douglas Paul
Vice President & Partner
Medical Marketing Economics, LLC
 
Ian Phillips
Norris Professor of Life Sciences & Director of the Center for Rare Disease Therapies Faculty Director
Keck Graduate Institute
 
Philip Vickers
Senior Vice President, Research and Development
 
Deadline for Abstracts: Jan 8, 2013
 
Registration: Register by March 8, 2013 for a 20% Discount. Or Register 3 for the price of 2 with the coupon code rcdvb!
E-mail: infogtcbio@gtcbio.com
 
   
 
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