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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


EVENTS

May 18 - 21, 2013

Medpace will attend Digestive Disease Week in Orlando.

May 20 - 22, 2013

Medpace will speak at the Global Clinical Trials Outsourcing Summit in Seoul.

May 22 - 23, 2013

Medpace will speak at Partnerships in Clinical Trials Russia in Istanbul.

May 23 - 24, 2013

Medpace will sponsor the Neurotech Investing & Partnering Conference in St. Regis San Francisco.

May 28 - 31, 2013

Medpace will attend the New Clinical Drug Evalutation Unit Annual Meeting (NCDEU) in Hollywood.

May 29 - 30, 2013

Medpace will attend the New York Biotechnology Association (NYBA) Annual Meeting in New York City.

May 31 - June 4, 2013

Medpace will exhibit at the American Society of Clinical Oncology (ASCO) Annual Meeting in Chicago.

June 2 - 5, 2013

Medpace will attend the 81st Congress of the European Atherosclerosis Society in Lyon.

June 12 - 13, 2013

Medpace will exhibit at Outsourcing in Clinical Trials: Medical Devices & Diagnostics in St. Paul.

June 12 - 13, 2013

Medpace will attend Anglonordic Medtech Conference II and Anglonordic Biotech Conference X in London.

June 21 - 25, 2013

Medpace will exhibit at the American Diabetes Association's 73rd Scientific Sessions in Chicago.

June 23 - 27, 2013

Medpace will exhibit at the DIA Annual Meeting in Boston.

July 17 - 18, 2013

Medpace will exhibit at Clinical Operations in Oncology Trials USA in Boston.



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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

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.

Events

May 18 - 21, 2013
Digestive Disease Week
Orlando, US

May 20 - 22, 2013
Global Clinical Trials Outsourcing Summit
Seoul, Korea

May 22 - 23, 2013
Partnerships in Clinical Trials Russia
Istanbul, Turkey

May 23 - 24, 2013
The Neurotech Investing & Partnering Conference 2013
St. Regis San Francisco, US

May 28 - 31, 2013
New Clinical Drug Evalutation Unit Annual Meeting (NCDEU)
Hollywood, US

May 29 - 30, 2013
New York Biotechnology Association (NYBA) Annual Meeting
New York City, US

May 31 - June 4, 2013
American Society of Clinical Oncology (ASCO) Annual Meeting
Chicago, US

June 2 - 5, 2013
81st Congress of the European Atherosclerosis Society
Lyon, France

June 12 - 13, 2013
Outsourcing in Clinical Trials: Medical Devices & Diagnostics
St. Paul, US

June 12 - 13, 2013
Anglonordic Medtech Conference II and Anglonordic Biotech Conference X
London, UK

June 21 - 25, 2013
American Diabetes Association's 73rd Scientific Sessions
Chicago, US

June 23 - 27, 2013
DIA Annual Meeting
Boston, US

July 17 - 18, 2013
Clinical Operations in Oncology Trials USA
Boston, US



REQUEST A MEETING

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
Videos



Podcasts/webcasts
US Medical Device Regulations and Regulatory Landscape Mike Winegar
Vice President Regulatory Affairs, Medpace Medical Device

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QT Evaluation in Early Clinical Development Thomas Todaro, MD, JD, FACC
Medpace Vice President, Medical Affairs

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