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Phase IIb-IV
GENERAL CAPABILITIES

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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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Strategic Partners

Experience has taught us that effective and consistent communication between the Sponsor, investigator and research sites, patients, and the Clinical Research Organization (CRO) is integral to the success of every clinical trial. It's a matter of how we think about drug development at Medpace – we recognize that development time is crucial and we believe that partnering leads to projects being delivered quickly, efficiently, and cost effectively. This unique partnering philosophy is what drives us – we know how to successfully manage our partners' projects and our infrastructure is designed to leverage this knowledge to proactively deliver superior insight, strategy, and efficiencies to each and every phase of trial. At Medpace, we build long-term relationships that ensure results.

Sponsor Partnerships

Medpace shares a common goal with our Sponsors – advancing drugs from development plan to regulatory approval in the most accurate, efficient, and cost-effective manner. Our Sponsors seek a dedicated partner who can engage quickly and provide strategic thinking. Every Medpace project team is structured to serve as an extension of your team. Every partnership is designed to create research solutions focused on your unique clinical trial. Led by the industry's top therapeutic and regulatory experts, our proficient and experienced employees are committed to providing you with best in class service and unrivaled support at every stage of the drug development process.

Investigator and Research Site Partnerships

The success of clinical trials is measured in terms of data quality, speed, and cost effectiveness – Medpace recognizes that partnering with the right investigators to meet recruitment challenges across all research sites is critical to this success. We know what's most important to investigators – good protocol design, project planning and organization, and open, effective communication. With medical and regulatory expertise in drug development in multiple therapeutic specialties, we apply our extensive experience working with thousands of investigators and research sites around the world. Our therapeutically-focused Clinical Research Associates are dedicated to an average of only two projects at a time so they can concentrate on process excellence, training research site personnel, and ensuring that everyone is focused on your unique clinical trial. As a result, we have developed consistent, longstanding, and positive partnerships with each of our research sites.

Patient Partnerships

Medpace places a high value on study participant relationships. Patient volunteers are essential to the success of the drug development process, without them it would be impossible to research new medical treatments that have the potential to improve the quality of life. Led and trained by the top medical experts in the industry, Medpace has an uncompromising commitment to the highest level of ethical standards and safety. We make sure patients are always treated with respect and consideration and have reliable and accurate information throughout the study.

Services

  • Clinical Operations
  • Medical Writing
  • Biometrics
  • Regulatory Affairs
  • Quality Assurance
  • Pharmacovigilance
  • Adjudication Services
  • ClinTrak Technology (IVRS/IWRS)
  • Cardiovascular Core Laboratory
  • Imaging Services
  • Pharmacokinetics
  • Central Laboratory
  • Bioanalytical Services