Medpace is a global, research-based drug development company led by top scientists and regulatory experts who are driven to further the advancement of pharmaceuticals in the areas of cardiology, metabolism, and oncology. With an unparalleled commitment to "best in class" science, Medpace has assembled one of the industry’s most experienced and specialized medical teams to oversee every level of the company’s clinical operations, providing complete and seamless drug development services.

With more than 500 employees and clinical trial experience in 40 countries, Medpace has the global reach and capability to conduct studies and navigate regulatory requirements worldwide.

Through its specialized scientific and regulatory expertise and medically focused clinical operations, Medpace provides the pharmaceutical and biotechnology industries with the most efficient and cost-effective path to drug approval - from program development to product approval.

The Medpace approach creates a therapeutically focused project team, increasing the quality of every service, including the following:

• Medical Expertise
• Regulatory Affairs
• Safety/Pharmacovigilance
• Clinical Operations
• Data Management
• Biostatistics
• Quality Assurance
• Medical Writing
• Cardiac Safety
• Interactive Voice Response System

• Cardiology
• Endocrinology
• Metabolism
• Oncology

Africa, Asia/Pacific, Australia, China, Eastern Europe, India, Latin America, the Middle East, North America, and Western Europe

Medpace Clinical Pharmacology Unit
The Medpace Clinical Pharmacology Unit (Medpace CPU) is a state-of-the-art Phase I, IIa facility with a core ECG lab focusing on confined/controlled pharmacokinetic/pharmacodynamic studies utilizing human volunteers, with first-in-man capability.

Medpace Reference Laboratories
Medpace Reference Laboratories (MRL) is a central laboratory with locations in Leuven, Belgium, and Cincinnati, USA. The expertise within Medpace Reference Laboratories includes coagulation, cardiovascular diseases, oncology, lipids, diabetes, and other metabolic diseases.

Medpace Reference Laboratories offers clients analytical support during all stages of the drug development process, with more than 65,000 square feet dedicated to laboratory operations and specimen storage. Preparation, packaging, and delivery of all supplies and materials necessary for specimen collection are also managed within the laboratory facilities.

Imagepace
Imagepace provides a comprehensive group of services designed to seamlessly integrate imaging studies into the complex structure of a clinical trial. The Imagepace team brings clinical trial experience and discipline to the management of imaging processes to ensure that imaging study results are valid, controlled, and easily integrated into overall clinical trial study results.

Imagepace is the world leader in cIMT imaging with a network of ultrasound imaging sites and a coordinated data processing and management system, Imagepace utilizes standardized cIMT technology to conduct clinical trials with a cIMT endpoint.

Medpace - Phases IIb, III, IV clinical development
Medpace Clinical Pharmacology Unit (Medpace CPU) - Phases I, IIa clinical development
Medpace Reference Laboratories (MRL) - Centralized laboratory specializing in cardiovascular and metabolic studies
Imagepace - Imaging core laboratory providing centralized image management, and reading.

For more information about Medpace or to receive a project proposal, please contact John Wynne at 513-579-9911 or toll-free at 1-800-730-5779.

For an exciting career move, visit www.medpace.com and review our open positions in our career section.

Global Headquarters - USA
Medpace
4620 Wesley Avenue
Cincinnati, OH 45212
Tel: 513-579-9911
Fax: 513-579-0444
www.medpace.com

Contact Information

Medpace, Inc.
John Wynne
4620 Wesley Avenue
Cincinnati, OH 45212 USA
Phone: 513-579-9911
Fax: 513-579-0444
E-mail:

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