Leverage our end-to-end PGx solutions for clinical trials

Drug Research Laboratory

Leverage our end-to-end PGx solutions for clinical trials

A trustworthy PGx Laboratory Partner

Pharmacogenomics (PGx) testing is an increasingly important tool for clinical trial enrollment, interpretation of clinical data and retrospective studies. We offer PharmacoScanTM assay, custom genotyping panel, and next generation sequencing (NGS) services for clinical trials and drug development. RPRD is a recognized leader in precision medicine research and clinical testing, bringing deep expertise and an unparalleled testing and data analysis service to organizations conducting clinical trials and drug development.

Precision Medicine Scientists
  • Fully CLIA-certified diagnostic testing laboratory
  • 100% pass rate on CAP proficiency testing
  • A full portfolio of genetic technology platforms, including next generation sequencing (NGS), microarray, real time PCR, etc.
  • Years of experience in developing high quality custom assays using various technologies, including Ampliseq, OpenArrayTM, etc. 
  • HIPPA compliant secure data transfer and reporting 
  • 100% customer satisfaction guaranteed 
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High Quality Testing Service and Support

We are committed to offer the best quality testing and unparalleled supporting service, using NGS, PharmacoScanTM , real time PCR, etc.

  • Most comprehensive coverage of PGx genes and alleles
  • Thorough analysis of SNPs, Indels, CNVs, translocations, etc.
  • High specificity and accuracy guaranteed
  • End-to-end quality control system including hands-on curation by PGx experts to ensure high quality calls
  • A dedicated project manager supporting the whole project
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Customized, end-to-end PGx solutions

We offer customized and end-to-end precision medicine solutions by leveraging our decades of experience in genomics translational research and clinical testing. We specialize in high-quality data analysis and clinical interpretation to help our partners develop better therapies for tomorrow. We provide precision medicine consulting services at each stage of a project to help guide our partners during the development process.

  • Any PGx research questions
  • Any stage of the clinical study
  • Any Scope of Work
  • Any number of samples
  • Any sample type (whole blood samples, saliva, buccal swab, etc.)
  • Consulting at every stage of your project by our PGx experts 
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State-of-the-art PGx technologies

We offer comprehensive genomic profiling of clinical trial samples in our CLIA-certified laboratory utilizing our comprehensive genomic profiling tests based on NGS and the PharmacoScanTM platform.

Read more about our expertise in NGS.


PharmacoScanTM is an ideal genotyping platform for translational researchers in pharma and research organizations looking to understand how genetic variations affect drug absorption, distribution, metabolism, and excretion (ADME).

We can precisely and reproducibly analyze 4,627 biomarkers within nearly 1,200 genes.

The solution includes detecting copy number variation (CNV) and interrogating predictive markers in complex genes (e.g. CYP2D6).

Unlike other platforms that analyze only the common markers, our comprehensive testing approach presents a more complete view of genotype information that potentially lead to more accurate PGx risk evaluation.


PharmacoScan™ Assay Kit: www.thermofisher.com/order/catalog/product/903026

Leverage our End-to-End Solutions Today

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