Versiti Clinical Trial Services is composed of multiple specialty organizations optimized to support the development of Companion Diagnostic (CDx) assays for therapeutic advancement. We understand the full clinical trials ecosystem and seamlessly integrate assay development, regulatory pathway mapping, and project and data management to deliver actionable, batched data—on time, every time. Because patients are waiting, we work with urgency to accelerate the path from development to impact.
Versiti understands the critical need to identify patient match and benefits from therapeutic treatment in the drug development and clinical trials ecosystem. Our experience translating the latest scientific discoveries into specialized diagnostic testing provides clients and trial patients with the latest, most accurate tools for screening, enrolling, and monitoring patients.
Services and Approach
Versiti Diagnostic Lab experts are highly skilled in an array of technologies, including DNA sequencing, gene expression, genotyping, flow cytometry and ELISA. Whether your project includes testing a handful of samples or thousands, we are equipped with multiple platforms to reliably meet different throughput requirements. Our team delivers dependable, quality solutions for both preclinical and clinical studies.
Our clinical trial methodology includes proactive processes to understand your goals, rapid and responsive communication, and prompt turnaround times. Our assay development processes include expert medical and scientific consultation to ensure your project is executed to your desired specifications, following best practices.