Your diagnostics, our expertise: custom CRO services built for qPCR and NGS workflows
At MicroVerix, our Contract Research (CRO) Services are built around one principle: diagnostics must work in the real world, not just on paper. We partner with assay developers, biotech companies, and clinical labs to deliver custom research, validation, and analytical performance studies aligned with CLIA, ISO 13485, and FDA QSR requirements.
Our CRO expertise spans end-to-end assay validation, including:
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Whole-organism control studies that replicate patient sample complexity.
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Limit of detection (LoD), specificity, cross-reactivity, and reproducibility testing for both qPCR and NGS panels.
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Custom microbial challenges, including rare, emerging, and multidrug-resistant organisms.
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Regulatory-ready data packages to support submissions and accreditation.
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Clinical Validation Pathway – With these controls, labs can robustly measure LoD, specificity, cross-reactivity, reproducibility, and bioinformatics accuracy—key metrics for regulatory submissions and accreditation.
With facilities and collaborators in both the US and India, MicroVerix combines global reach with agile execution, offering cost-effective solutions that are scalable for high-throughput labs and resource-limited settings alike. Whether you need a partner for precision metagenomics validation, AMR marker testing, or custom syndromic panels, our CRO services provide the depth, flexibility, and scientific rigor to move your innovations forward.