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ASBM Releases Findings of European Prescriber Survey in Brussels

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ASBM Presents at WHO Meeting on Naming

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Dolinar presents at NALEO Health Summit

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ASBM Participates in Biosimilars Discussion in Mexico City

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State Legislation on Substitution

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Europe Approves First Biosimilar Monoclonal Antibodies

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FDA Guidance on Biosimilars

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The Issue: Putting Patients First

Biologics are advanced prescription drugs to treat cancer, rheumatoid arthritis and other debilitating diseases. As early as 2014, the first attempts to copy these drugs, known as biosimilars, are expected to be approved. Since 2010, The Food and Drug Administration has been consulting patient groups, physicians and industry on how to best ensure safe access to these powerful medicines. The Alliance for Safe Biologic Medicines works ensure patient safety remains the priority, submitting formal comments to FDA in February of 2012, and its members testifying at an FDA hearing in May 2012 and before several state legislatures, and conducting educational forums nationwide. LEARN MORE

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The Alliance for Safe Biologic Medicines is an organization composed of diverse healthcare groups and individuals—from patients to physicians, biotechnology companies that develop innovative and biosimilar medicines and others who are working together to ensure patient safety is at the forefront of the biosimilars policy discussion.Read More

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