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VacChina 2011 - Bridging the China Vaccine Industry with the World Class Biotechnologies
Date:8/18/2011

working mechanisms
  • How to align China SFDA's regulatory pathways and domestic clinical trials with international standards and requirements
  • What do new Chinese Good Manufacturing Practice (GMP) standards and WHO approval for China's vaccine regulatory system mean for China's vaccine industry? Now that Chinese vaccine manufacturers can apply for WHO prequalification, will China take on a bigger role as a global vaccine supplier? Should we expect China to take a larger role developing novel vaccines?
  • What kind of assistance do SFDA, CDC and Chinese manufacturers need from international partners (WHO, UNICEF, PATH, etc) to improve and meet international standards? How will China respond to international concerns about quality and safety of Chinese vaccines?
  • Novel approaches to cell culture to accelerate development and quality control
  • How to improve cost and time to the clinic and ensure product quality through downstream processing
  • Strategies to accelerate vaccine development process with the latest expression and characterization technologies

  • For more information, please visit vac.globaleaders.com or contact:

    Daniel Chen
    Tel: +86-21-3251-6046 or email: daniel.chen@globaleaders.com


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    SOURCE Global Leaders Institute
    Copyright©2010 PR Newswire.
    All rights reserved

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