Medpace has the global reach and capability to conduct studies in biopharmaceuticals and medical device - assisting sponsors with regulatory requirements. We also help deliver custom solutions specific to your needs on six of the seven continents. Projects are facilitated through regional offices located throughout Europe, Asia, Australia, South Africa, and the Americas, with staff and offices continually added throughout the world. Integration of Clinical Pharmacology, Central Laboratory, Imaging, and Bioanalytical capabilities into the design of a clinical trial allows Sponsors the most efficient global trial conduct from discovery to post marketing.

Medpace experts have a deeper understanding of local language, culture, and processes, creating better relationships with investigators and improved trial execution. They have greater access to the country patient populations for faster enrollment timelines and lower costs.

The Medpace expanding global footprint is interconnected through our innovative suite of technologies, ClinTrak®, which gives sponsors and study managers real-time access to critical study data, supporting project decisions on a global level.