Stay Connected
Join us on Facebook Follow us on linked in Follow us on YouTube Follow us on Vimeo
Main Services of Medpace
What We Do

Want to learn more about our customized services? Simply fill out this form and we will contact you.


VIEW NOW View now

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:

Want to learn more? Contact the location nearest you.


February 22-23, 2017 Outsourcing in Clinical Trials West Coast 2017 in Burlingame

March 21-23, 2017 2017 BioPharma Asia in Singapore

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

GO NOW more