Globalization of Biosimilars

Global uptake of Biosimilars has led to the adoption of distinct legal and regulatory frameworks in different countries. Thorough understanding of the marketing strategies, newer analytical characterization techniques and proper communication between regulatory authorities and manufacturers may help to bring a biosimilars more easily in the global market.

South Korea was the first country worldwide to approve biosimilar versions of etanercept according to international standards. Australia is the world’s first highly regulated market to allow pharmacy level substitution of a monoclonal antibody biosimilar for an originator. As of April 2016; 8 biosimilars have been approved in Japan, including the recent approved insulin glargine biosimilar. A recent report has shown that biosimilars in India have witnessed nearly 20% annual growth for the last financial year and now make up for about 2.5% of the overall biologics market.

  • Global uptake of Biosimilars
  • Global impact of biosimilars over generics
  • Biosimilars in global market
  • Investment and returns on biosimilars
  • Cost and risk management
  • Adopting innovative mechanisms such as risk-sharing arrangement
  • Global P&R models for the biosimilars and generics market

Related Conference of Globalization of Biosimilars

July 03-05, 2017

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8th Asian Biologics and Biosimilars Congress

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10th Pharmacovigilance Congress

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7th International Conference and Exhibition on Pharmaceutical Regulatory Affairs and IPR

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6th International Conference and Exhibition on GMP, GCP & Quality Control

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World Congress on Antibiotics: R&D, Market

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12th World Pharma Congress

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October 16-18, 2017

11th World Drug Delivery Summit

(10 Plenary Forums - 1Event)
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10th International Conference and Exhibition on Biologics and Biosimilars

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4th European Biopharma Congress

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7th Global Mass Spectrometry Congress

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Globalization of Biosimilars Conference Speakers

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