Global Capacity
Medpace provides true device expertise with over 1000 employees and 18 offices worldwide, providing coverage
for clinical trials in over 40 countries. Whether you are launching your CE mark trial or a global pivotal
trial for PMA approval, we can help you navigate the regulatory landscape and leverage our global
infrastructure for the highest quality results.
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Device Expertise
Our dedication to medical device trials, best-in-class clinical trial management processes,
and customer focused philosophy position us as a strategic partner to help you complete your
clinical trial on time and on budget. Our relationships with investigators and clinical sites
with therapy specific device trial experience allow us to deliver results.
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Integrated Capabilities
The ability of Medpace experts to integrate Clinical Trial Management, Central Laboratory, Imaging, and
Clinical Database capabilities together into one coordinated project allows Sponsors the most efficient
trial conduct from start to finish without skipping a beat.
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