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Featuring case studies and presentations from:
Lee Chichang
Executive Director, Simcere
Pharmaceuticals, China
Paul Kim
Head, Novartis Korea
Venture Fund
Paik Sang Hoon
Chief Research Scientist / Team
Leader, Cell Culture Process
Development Team, Green
Cross Corporation, Korea
Gerhard Klement
Director Pharma Solutions,
Piramal Healthcare, India
Jian Dong
Vice President Manufacturing,
Shanghai Kanda Biotech,
China
Jason Li
Director, P&PD Purification Department, Wison, China
Dr Jin Yin
Principal Engineer, Cell Culture
Process Development, Shire
Human Genetic Therapies,
USA
Dr Shivraj Dasari
Vice President Quality Management and Regulatory Affairs, Innobioventures, Malaysia
Hyukjong Lee
Managing Director, Binex
Pharmaceuticals, Korea
Arvind Kushwaha
Head, DSP (Production, Intas
Biopharmaceuticals, India
Jerold Martin
Chairman of the Board,
Bio-Process Systems Alliance
(BPSA), USA, Sr. Vice President, Global Scientific Affairs,
Pall Life Sciences, USA
Lei Sun
President, Manufacturing Business, Autekbio, China

7 Reasons Why You Should Attend:
  • Gain valuable insights from international and regional industry leaders
  • Assess the impact of regulatory reforms on disposable systems in biomanufacturing
  • Gather updates on the latest global biomanufacturing technology and applications
  • Maximise efficiencies with practical examples of process development & operations in disposable biomanufacturing
  • Ensure the right mechanisms are in place for efficient biomanufacturing in Asia
  • Understand the concepts of disposable technology and analyze costs / benefits for single-use systems
  • Mitigate operational and quality risk within manufacturing design and operations by implementing best practices

Key themes and issues to be discussed include:
  • Creating Fertile Conditions for Biomanufacturing to Flourish in Asia
  • Examining Long Term Benefits and the Real Cost of Single Use Systems
  • Bringing Downstream Productivity on par with Upstream Efficiency
  • Charting the Future of Biomanufacturing in Asia

PLUS! Pre-Conference Workshops: 7 March 2011
Workshop A: Understanding Regulatory Affairs for GMP and
Biomanufacturing
Workshop B: Cleaning Validations for Biopharmaceuticals



 
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