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.