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Main Services of Medpace
What We Do

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Established in 1992, Medpace partners with leading pharmaceutical, biotechnology, and medical device companies to bring promising new drugs to market. As a full-service Clinical Research Organization (CRO), we combine efficient clinical trial management, comprehensive regulatory consulting, and innovative technologies to create a customized approach that ensures powerful solutions for our partners around the globe.

Led by therapeutic experts with extensive experience in the advancement of pharmaceutical agents for use in multiple therapeutic specialties, Medpace's dedicated teams deliver rapid and accurate clinical trial results for the most complete Phase I-IV clinical research support in the industry. Our regulatory experts; former government officials with valuable international insight into specific areas of drug approval are involved at project initiation, allowing them to develop an accurate description of your data to ensure that every phase of trial is precisely focused for maximum results.

Regardless of project size, Medpace has the breadth, depth, experience, and flexibility to deploy a study on six continents.

Our full-range of integrated and customized services includes:

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April 20-22, 2016 World Orphan Drug Conference in Washington D.C.

April 25-27, 2016 Diabetes Summit 2016 in Boston

request info Medpace is ready to help you with your next clinical trial project. Find out more about how we can help.

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