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Updated: Jul 5, 2026

Implementation of In Vitro Drug Resistance Assays: Maximizing the Potential for Uncovering Clinically Relevant Resistance Mechanisms
Published on: December 9, 2015
A review of public policy issues in promoting the development and commercialization of pharmacogenomic applications:
Louis P Garrison1, Rick J Carlson, Josh J Carlson
1Department of Pharmacy, University of Washington, Seattle, Washington 98195, USA. lgarrisn@u.washington.edu
Abstract:
This article reviews the regulatory, social, policy, and other issues that will shape the development of pharmacogenomics applications. We identify and analyze 19 key public policy issues, ranging from the economic incentives for linked diagnostic-drug development, to the regulation of tests and drugs, and to privacy and informed consent. Challenging technical, business, and policy-related issues might either hinder progress in the field of pharmacogenomics or potentially accelerate it, depending on how they are addressed and resolved. How well the numerous important stakeholders - both private and public - address these issues will be critical for pharmacogenomics to deliver on its promise.
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