Medpace

About Medpace

Medpace is a global clinical research organization (CRO) that provides comprehensive drug development services to the pharmaceutical and biotechnology industries. Established in 1992, the company has built a reputation for excellence in clinical trial management and regulatory consulting.

With a focus on delivering high-quality data and efficient study execution, Medpace supports clients through every phase of the drug development process. The company’s services include:

• Clinical Trial Management: Medpace manages all aspects of clinical trials, ensuring compliance with regulatory requirements and adherence to timelines.
• Regulatory Affairs: The team provides expert guidance on navigating complex regulatory landscapes, helping clients achieve successful product approvals.
• Data Management: Medpace employs advanced technologies to ensure accurate and timely data collection and analysis.
• Biostatistics: The biostatistical team offers robust statistical support to enhance the integrity of clinical trial results.

Headquartered in Cincinnati, Ohio, Medpace operates globally, with offices in various countries, including the UK. The company prides itself on its commitment to quality, integrity, and collaboration, fostering strong partnerships with clients to drive innovation in healthcare.

Medpace’s vision is to be the leading provider of integrated drug development services, dedicated to improving patient outcomes and advancing medical science. By leveraging its extensive expertise and resources, Medpace aims to accelerate the delivery of new therapies to market, ultimately benefiting patients worldwide.