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3rd annual European Stem Cells & Regenerative Medicine Congress 2008
 
Conference:
Pre-congress briefing day
13th May 8.30am - 5:30pm
Day One
14th May 8.30am - 5:30pm
Day Two
15th May 8.30am - 5:30pm

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conference discounts
Terrapinn is offering a 50% discount for academia / government / not-for profit representatives. 
 
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Translating stem cell research from bench to business
 

The global market for stem cell products and services is forecast to grow almost threefold by 2010 and stem cell research continues to make significant advances towards valuable medical treatments. Despite these advances, the development of stem cell products remains a virtually untapped profit centre. The 3rd annual European Stem Cells & Regenerative Medicine Congress focuses on bridging these gaps between researchers, investors and manufacturers. The focus is both scientific and commercial. This 3-day event will represent the pioneering work being conducted by 50 of the world's most respected research and commercial organisations.

The congress has been shaped to appeal to senior level executives, providing you with the resources, information and advice you need to aid your research, strategic business planning, decision making and your future professional development.

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“Great cross section of vaccine science, excellent speakers, well organised format.  I would definitely recommend.”  Annie DeGroot, CEO, EpiVax

 

This year's speakers include:
 

Dr Alan Trounson
President
California Institute of Regenerative Medicine

Mr Bernard Siegel          Executive Director
Genetics Policy Institute
Dr Thomas Okarma        Chief Executive Officer
Geron
Dr Gail Naughton
Chief Executive Officer
Histogen

Dr Eric Lagasse
Professor, Department of Pathology and Director of the Cancer Stem Cell Center
McGowan Institute for Regenerative Medicine

 
Dr. Michael West
Chief Executive Officer
Biotime

 

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Key topics include:
  • Stem cell development: emerging into a competitive marketplace
  • Funding and operation: securing investment for stem cell businesses
  • Expansion of clinical automation processes
  • Multi-phase clinical trials in therapeutic stem cell applications
  • Motion towards therapeutic stem cell research
  • Developments within the regulatory, IP and reimbursement landscape
  • Contract manufacturing: scaling-up and developing a profitable business model for post-clinical operation
  • The necessity for an international industry association for regenerative medicine
  • Stem cells in drug discovery and toxicity

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