Medpace is ready to help you with your next clinical trial project. Find out more about how we can help.
April 28 - 30, 2014
Medical World Americas Conference & Expo in Houston
April 30 - May 3, 2014
American Pain Society (APS) in Tampa
May 3 - 6, 2014
Digestive Disease Week in Chicago
May 7 - 9, 2014
Evolution Summit in Palm Beach
10 - 13 May 2014
European Congress of Clinical Microbiology and Infectious Diseases (ECCMID) in Barcelona
May 13 - 14, 2014
Outsourcing in Clinical Trials East Coast in Philadelphia
20 - 23 May 2014
EuroPCR in Paris
21 - 22 May 2014
Outsourcing in Clinical Trials Europe in Brussels
May 30 - June 3, 2014
ASCO Annual Meeting in Chicago
Visit Booth #8043
May 31 - June 3, 2014
European Atherosclerosis Society Congress in Madrid
May 31 - June 4, 2014
ISPOR International Meeting in Montreal
Request a Meeting
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5375 Medpace Way
Cincinnati, Ohio 45227
The advantage of Medpace.
A global leader in research-based drug and device development, Medpace builds strong strategic partnerships with select Sponsors to advance the most efficient and cost-effective path to drug and device approval. As a therapeutically-focused Clinical Research Organization (CRO), we view ourselves as stewards of your drug and device, leveraging our extensive medical and regulatory expertise to deliver additional input, strategy, and efficiencies to each and every phase of the clinical trial. From addressing the needs of small and midsize biotechnology companies to full-service offerings for global pharmaceutical companies, Medpace has the breadth, depth, and flexibility to deliver a superior result, specific to your needs, on six continents.
The advantage of expertise.
Led by top therapeutic and regulatory experts with extensive experience in the advancement of
pharmaceutical agents for use in multiple
therapeutic specialties, Medpace has cultivated a culture of expertise. Following our unique partnering philosophy, our dedicated teams serve as an extension of your team, ensuring unmatched expediency from start to finish. Before we even begin a trial, the Medpace proactive industry experts are already working on the right answers to streamline your development process and accelerate time to product approval. With an enviable track record of regulatory submissions around the globe, it's no wonder our partners view Medpace as a trusted advisor for the entire clinical development process.
The advantage of global reach.
Medpace is a privately held company with corporate headquarters in Cincinnati, OH; and 30 offices including laboratories throughout Europe, Asia, the Middle East,
Australia, Africa, and the Americas. Our expanding
global reach is interconnected through an innovative suite
of proprietary technologies, ClinTrak®, a study management system facilitating team coordination and
providing decision support for sponsors and sites, to ensure global teams are focused and organized for
maximum efficiencies using a common data platform. Clintrak provides near real time access to critical study
data, including lab and imaging information pertaining to the study.
The advantage of focus.
Real solutions demand the right people to do the right work. Anyone can assign people to work on a project, but only Medpace brings experienced minds to every phase of your project. It's a matter of how we think about drug and device development – ensuring powerful solutions demands focus. Advancing your drug or device from development plan to regulatory approval in the most efficient and cost-effective manner demands a concentrated effort every step of the way. Your success demands Medpace.
Want to learn more? Contact the Medpace location nearest you.