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March 23rd, 2005
Covance and Expression Analysis Team to Provide Genomic Microarray Testing Services for Clinical Trials
Release of the United States Food and Drug Administration (FDA) guidance document on pharmacogenomics data submissions indicates that genomic data may become a necessary component for regulatory submissions in the future.

October 26th, 2004
Covance Expands Singapore Central Laboratory with Nucleic Acid Amplification Testing Unit to Service Asian Trials
The addition of this laboratory testing service enables Covance to provide in-region, near real-time, nucleic acid amplification testing required by pharmaceutical and biotechnology companies to support their clinical trials in viral infectious diseases.


Article Reprints
May 2005
FDA offers pharmacogenomics data submissions guidelines
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