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Contract Research Organization providing Phase I-IV core development 
services for drug, biologic, and device programs
Medpace - A Therapeutically focused, trusted, global CRO
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Medpace is ready to help you with your next clinical trial project. Find out more about how we can help.

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GENERAL CAPABILITIES


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Medpace, Inc.
5375 Medpace Way
Cincinnati, Ohio 45227
USA
Toll-free: +1.800.730.5779
Tel: +1.513.579.9911
Fax: +1.513.579.0444
E-mail: info@medpace.com



EVENTS

September 5 - 9, 2014

Interscience Conference on Antimicrobial Agents and Chemotherapy (ICAAC) in Washington

Visit booth #1029

September 13 - 17, 2014

Transcatheter Cardiovascular Therapeutics (TCT) in Washington

September 14 - 17, 2014

18th Annual Scientific Meeting of the HFSA in Las Vegas

15 - 19 September 2014

50th EASD Annual Meeting in Vienna

26 - 30 September 2014

ESMO 2014 Congress in Madrid

October 7 - 8, 2014

Stem Cell Meeting on the Mesa in La Jolla

7 - 11 October 2014

World Muscle Society Congress in Berlin

October 8 - 12, 2014

IDWeek in Philadelphia

October 11 - 14, 2014

American Academy of Pediatrics Experience in San Diego

October 18 - 22, 2014

UEG Week in Vienna



VIEW ALL EVENTS

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.