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Between the Lines: Diving Deeper Into the EMERALD Trial

Opinion|Videos|February 1, 2025

One Institution’s Evidence-Based Approach to Adopting Biosimilars

Author(s)Eric Tichy, PharmD, MBA, BCPS, FCCP, FAST

A panelist discusses how their institution evaluates biosimilars for formulary inclusion through a systematic review process that examines clinical data, safety profiles, and cost implications while prioritizing operational efficiency, patient access, and seamless transitions between reference products and biosimilars.

Episodes in this series

EP. 1 One Institution’s Evidence-Based Approach to Adopting Biosimilars

EP. 1 One Institution’s Evidence-Based Approach to Adopting Biosimilars

EP. 2 Decision-Making and Evidence Evaluation of Biosimilars

EP. 2 Decision-Making and Evidence Evaluation of Biosimilars

EP. 3 Financial and Operational Considerations of Implementing Biosimilars

EP. 3 Financial and Operational Considerations of Implementing Biosimilars

EP. 4 Stakeholder Management and Interoperability of Biosimilars

EP. 4 Stakeholder Management and Interoperability of Biosimilars

EP. 5 Looking Ahead: Strategic Planning for Biosimilar Integration

EP. 5 Looking Ahead: Strategic Planning for Biosimilar Integration

EP. 6 Perspectives and Future Directions in Biosimilar Health Care Delivery

EP. 6 Perspectives and Future Directions in Biosimilar Health Care Delivery

EP. 7 Optimizing Biosimilar Implementation: A Framework for Access, Adoption, and Sustainability | Written Recap

EP. 7 Optimizing Biosimilar Implementation: A Framework for Access, Adoption, and Sustainability | Written Recap

Video content above is prompted by the following:

Please describe the process your institution uses to review biosimilars as potential additions to the formulary.
What priorities were identified by your institution for the purposes of operationalizing the use of biosimilars?

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