4th Annual Biosimilars North America is organized by SMi Group and would be held during Nov 15 - 16, 2017 at Renaissance Woodbridge Hotel, Iselin, New Jersey, United States Of America.
The first biosimilar product launched in the US in 2015. Currently there are only 4 biosimilar products approved but the North Americas market 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.
This year, the conference will also explore significant developmental topics within the sector including the impact of FDA’s newly implemented biosimilar interchangeability guidelines, the US market access landscape, and biosimilars of orphan drugs.
Benefits of attending :
• Hear Sandoz talk on the FDA issuing the long awaited biosimilar interchangeability guidance.
• Explore complex Biosimilars and new technologies from MedImmune.
• Learn how to combat the legal, policy and commercial obstacles to the development and launch of Biosimilars with Momenta Pharmaceuticals.
• Gain insights from FUJIFIlM Diosynth Biotechnologies on Biosimilar latest development strategies and successfully bringing biosimilars to market.
• Examine the drug product and formulation developmentconsiderations for biosimilars with Oncobiologics Inc.
Key highlights 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 fo 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
• Hiten Gutka, Principal Scientist Formulation Development - Biosimilar Development, Oncobiologics Inc
• Patrick Robertson, Director, Program Design, FUJIFIlM Diosynth Biotechnologies.
Price:
Book by June 30: USD 1599
Book by September 29: USD 1799
Standard: USD 1899
Workshop: USD 499
Additional details will be posted as soon as they are available.