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Date: Monday, September 24, 2012 - 9:00 am
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There will be case studies from those who are both developing and distributing follow on biologics. With analysis of key trends in biologic pipelines, methods in clinical trials for biosimilar approval, a review of emerging markets, assessment of biosimilar manufacturing, post approval strategy and future forecasting for follow on biologics. SMi’s Biosimilars and Biobetters event will provide up to date information from key opinion leaders in the biologics industry with discussion and debate and opportunities for networking between CROs, CMOs, law firms, regulatory bodies, pharma and biotechs. If you are interested in speaking at the conference, please contact This e-mail address is being protected from spambots. You need JavaScript enabled to view it For sponsorship and exhibition opportunities, please contact This e-mail address is being protected from spambots. You need JavaScript enabled to view it Why should you attend this event?
Laura McKinley, Director Worldwide Regulatory Strategy, Pfizer Paul Greenland, EMEA Director of Biosimilars and Proprietary Marketing, Hospira Andrew Rankin, Head of Clinical Development, Teva Pharmaceuticals Our expert speaker line-up also includes: Sreedhar Sagi, Risk Management Compliance Officer Biopharmaceuticals Development, Sandoz |
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