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Renaissance Boston Waterfront Hotel, Boston, MA
August 19-23, 2013
Program Titles: - Optimizing Cell Culture Technology
- Facilities for Manufacturing Biologics
- Higher-Order Protein Structure
- Overcoming Formulation Challenges
- Optimizing Cell Line Development
- Scaling Up & Down with Optimized Bioreactors
- Rapid Methods to Assess Quality & Stability of Biologics
- High-Concentration Protein Formulations
- Early IND Strategies: Analytical Development
- Early IND Strategies: Process and Production
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Organized by:
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Cambridge Healthtech Institute |
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Invited Speakers:
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Keynote Speakers: - Thomas Ryll, Ph.D., Director, Cell Culture Development, Biogen Idec, Inc.
- R. Thomas Warf, Senior Program Manager, Product Process Development Analysis, Influenza and Emerging Diseases Division, Biomedical Advanced Research and Development Authority (BARDA), Office of the Assistant Secretary for Preparedness and Response, U.S. Department of Health and Human Services
- Palani Palaniappan, Ph.D., Vice President and Head, Biologics CMC, CMC Center, Millennium: The Takeda Oncology Company
- Florian M. Wurm, Ph.D., Professor, Chemistry Engineering & Cell Bio Lab, School of Life Sciences, Integrative Bioscience Institute, École Polytechnique Federale De Lausanne (EPFL), and Founder & CSO, ExcellGene SA
- Ravinder Bhatia, Ph.D., Associate Director, Pharmaceutical Development and Manufacturing Sciences, Janssen Research & Development
- Jianmei Kochling, Ph.D., Director, Quality Control Technical Services, Genzyme, a Sanofi Company
- Donna L. Luisi, Ph.D., Senior Principal Scientist, Pharmaceutical Research & Development, Pfizer, Inc.
- Thomas Laue, Ph.D., Professor, Biochemistry and Molecular Biology; Director, Biomolecular Interaction Technologies Center (BITC), University of New Hampshire
- Joanne Beck, Ph.D., Vice President, Process Development, Shire Human Genetic Therapies
To see a full speaker list, visit http://bit.ly/15TG0EW
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Deadline for Abstracts:
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July 19, 2013
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Registration:
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Register Now
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E-mail:
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kwaterman@healthtech.com
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