Medpace is a Contract Research Organization (CRO) that provides comprehensive clinical research services to accelerate the development of medical therapeutics. It's ideal for biotech companies seeking a streamlined approach to drug and biologic development. With over 30 years of experience, Medpace integrates scientific, regulatory, and operational expertise into its projects.

Key Features:

Therapeutic Expertise: Medpace employs a therapeutically-focused model, ensuring that sponsors receive insights from medical experts throughout trial design and execution.
Integrated Labs: Offers fully-integrated central and bioanalytical laboratory services, including imaging and ECG core labs, to support efficient trial execution.
Team Continuity: A single cross-functional team remains engaged throughout the project lifecycle, optimizing performance and ensuring high-quality results.
Global Reach: With resources across North America, Europe, Latin America, and Asia Pacific, Medpace navigates diverse regulatory environments and reaches targeted patient populations.
End-to-End Services: Provides a full-service model, coordinating all aspects of clinical research to increase quality and speed while reducing the need for duplicate oversight.

Medpace

Medpace offers integrated clinical research services for drug development, including laboratory and imaging services, ensuring efficient trial execution.

United States

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Key Features:

Therapeutic Expertise: Medpace employs a therapeutically-focused model, ensuring that sponsors receive insights from medical experts throughout trial design and execution.
Integrated Labs: Offers fully-integrated central and bioanalytical laboratory services, including imaging and ECG core labs, to support efficient trial execution.
Team Continuity: A single cross-functional team remains engaged throughout the project lifecycle, optimizing performance and ensuring high-quality results.
Global Reach: With resources across North America, Europe, Latin America, and Asia Pacific, Medpace navigates diverse regulatory environments and reaches targeted patient populations.
End-to-End Services: Provides a full-service model, coordinating all aspects of clinical research to increase quality and speed while reducing the need for duplicate oversight.