The Pharmacy Times® Biosimilars Resource Center is a comprehensive resource for clinical news and expert insights on issues related to biosimilar drugs, a biological product that is highly similar to a reference biologic for which there are no clinically meaningful differences in terms of safety, purity, and efficacy.
January 14th 2025
Successfully integrating biosimilars into practices requires careful planning and execution, as they impact virtually all aspects of a practice.
Governor Kitzhaber Signs Legislation to Create Pathway for Substitution of Biologic Drugs
June 7th 2013The Biotechnology Industry Organization (BIO) and Oregon Bioscience Association (Oregon Bio) commend Oregon Governor John Kitzhaber for signing legislation designed to address the regulatory issues related to the interchangeability of biological medicines.
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Illinois Strikes Down Biosimilar Legislation
June 6th 2013Illinois is now the 13th state to avoid enacting legislation that would slow patient access to biosimilars, which are new, affordable versions of costly brand biologic medicines that treat cancer, immune disorders and other complex diseases.
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Implications of Biosimilar Use: A Market Perspective
March 14th 2013The global market for biosimilars is predicted to grow to $3.7 billion by 2015, according to a recent report by Grant Thornton. Will proposed legislation regarding the interchangeability of biosimilars thwart United States innovation and leave us far behind our European counterparts?
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Managed Care Biologics and Injectables
February 17th 2012Payer response to new entrants to the multiple sclerosis (MS) market is mixed as some believe that there remain meaningful, major unmet needs in the MS category, according to The Zitter Group's Spring 2011 Managed Care Biologics and Injectables Index.
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