At CovarsaDx, our team of clinical research professionals, regulatory consultants, and quality assurance experts brings unmatched expertise in IVD and medical device clinical trials. With decades of combined experience, we support sponsors through every stage of the product lifecycle—from study design and FDA submissions to quality system implementation and post-market surveillance.
We’ve built a team that understands the regulatory complexities and operational challenges unique to diagnostics and medical devices. Our collaborative, cross-functional approach ensures that every sponsor receives tailored support, compliant processes, and exceptional service.
Ready to Partner with a CRO That Puts Expertise First?
The CovarsaDx team is committed to advancing diagnostic and device innovation through high-quality clinical research, regulatory clarity, and inspection-ready execution. Whether you need end-to-end IVD clinical trial support, regulatory guidance, or quality assurance services, our experts are here to help.
Learn how our team can support your next clinical study or regulatory submission.