Investigation of Nonproprietary Name Suffix Use for Biologics and Biosimilars

Project Title Investigation of Nonproprietary Name Suffix Use for Biologics and Biosimilars
Date Posted
Wednesday, April 24, 2019
Status
In progress
Description

The goal of this project is to understand the role of FDA’s nonproprietary name suffix in routine clinical care. Currently, there are several ways used by different federal agencies to identify biologics and biosimilars. This project will evaluate how one large institution identifies biosimilars in their systems, from the point of physician order entry through insurance coding and reimbursement.

Workgroup Leader(s)

Joshua Baker MD, MSCE; University of Pennsylvania School of Medicine, Philadelphia, PA

Sarah Dutcher PhD; Office of Surveillance and Epidemiology, Center for Drug Evaluation and Research, U.S. Food and Drug Administration, Silver Spring, MD

Lubna Merchant MS, PharmD; Office of Medication Error Prevention and Risk Management, Center for Drug Evaluation and Research, U.S. Food and Drug Administration, Silver Spring, MD

Workgroup Members

Charles Leonard PharmD, MSCE; Vincent Lo Re MD, MSCE; Judy Shea PhD; University of Pennsylvania School of Medicine, Philadelphia, PA

Susan Forrow BA; Department of Population Medicine, Harvard Pilgrim Health Care Institute and Harvard Medical School, Boston, MA

Medical Product
biologic
biosimilar
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