4th annual Biosimilars North America

Renaissance Woodbridge Hotel, Iselin, New Jersey, USA (November, 15 - 16, 2017)

The market for biosimilars in North America continues to grow and has become highly lucrative. As such, pharmaceutical companies continue to find ways to differentiate their products in such a saturated market. Thus, Biosimilars North America 2017 will provide an intelligent meeting to explore novel and innovative strategies to advance biosimilar development, and ensure optimal market access and commercialization opportunities whilst complying with evolving regulatory requirements.

Key highlights this year will include

·         A presentation from Sandoz on the FDA issuing the long-awaited biosimilar interchangeability guidance

·         A session on complex biosimilars and new technologies from MedImmune

·         Momenta Pharmaceuticals will provide strategies to combat legal, policy and commercial obstacles to development and launch

·         Insights on latest development strategies and market access from Fujifilm Diosynth Biotechnologies

·         A talk on drug product and formulation development considerations with Oncobiologics

Key speakers include

·         Richard DiCicco, Chairman, Harvest Moon Pharmaceuticals Inc

·         Cindy Cao, Executive Director & Head of US Regulatory Affairs for Biopharmaceuticals, Sandoz

·         T. Shantha Raju, Senior Director, MedImmune

·         Chrys Kokino, Head Global Biologics Commercial, Mylan

·         Steinar Madsen, Medical Director, Norwegian Medicines Agency

·         Bruce Leicher, Senior Vice President and General Counsel, Momenta Pharmaceuticals, Inc

·         Hiten Gutka, Principal Scientist Formulation Development - Biosimilar Development, Oncobiologics Inc

·         Patrick Robertson, Director, Program Design, FUJIFIlM Diosynth Biotechnologies

Více: http://www.smi-online.co.uk/pharmaceuticals/northamerica/biosimilars-n