A distinct advantage for Sponsors is the depth of therapeutic expertise that is unleashed on your trials. Unlike other CROs, our experts—from medical, operational, regulatory, laboratory and imaging--stay involved from early planning through execution to ensure your trial stays on pace.
Over 80 Medical Doctors and Advanced Clinical Practitioners work collaboratively to ensure your trial is scientifically and operationally sound.
A full-service, single-vendor outsourcing strategy provides built-in efficiencies and facilitates collaboration. This model is critical to our ability to streamline even the most complex global studies. In addition to end-to-end CRO services, Medpace’s wholly-owned Central Laboratories, Bioanalytical Lab, Imaging Core Lab, ECG Core Lab, and Phase I Unit, enable a deeper level of collaboration and efficiency.
With resources and expertise strategically located around the globe, Medpace skillfully navigates local languages, cultures and processes to avoid delays and missteps—delivering seamless execution amid the complex landscape of global clinical development.
Our 30-year history of purposeful, organic growth provides sponsors consistency in leadership, deep institutional experience, and incomparable efficiencies not found at other large or medium CROs. While others CROs have been busy merging – Medpace has been busy managing. This has resulted in a culture of quality that has not been disrupted by acquisitions. Medpace is a stable and predictable partner for advancing your compound.
30-Year - People. Purpose. Passion.
Driven by a full-service CRO model that coordinates and integrates all services for our clients, Medpace provides an accountable, seamless, integrated, and efficient platform for executing clinical research – increasing quality and speed while significantly reducing the need for duplicate management oversight. More than a “set of extra hands”, we are an extension of your team – embedding medical, regulatory and operational expertise into your trials to navigate and overcome challenges. It’s how we make the Complex Seamless™. And it’s why we are Trusted by Biotech™
Medpace employs a high-science and disciplined operating approach that leverages regulatory and therapeutic expertise across all major therapeutic areas. For sponsors, this means your clinical trial will be led by a collaborative team of medical, operational and regulatory experts with deep knowledge and insights about the disease and the patients your clinical trial is targeting. Backed by over 30-years of experience, our relationships with Key Opinion Leaders, Principal Investigators, and high-performing sites help accelerate clinical development.
When you partner with Medpace, you get guidance from our cross-functional team of experts who work together – combining our experience and perspectives – to guide and accelerate your compound through clinical development. This “cross-pollination” of experts from numerous functional areas—including medical, regulatory, operations, labs, and imaging—allows us to apply our experience and relationships to an extensive range of diseases. As a full-service CRO with labs, imaging, a phase I unit, and cardiac safety capabilities, we offer comprehensive services and the support of our collective expertise to accelerate your studies and programs.
When you partner with Medpace, you get guidance from our cross-functional team of experts who work together – combining our experience and perspectives – to guide and accelerate your compound through clinical development. This “cross-pollination” of experts from numerous functional areas—including medical, regulatory, operations, labs, and imaging—allows us to apply our experience and relationships to an extensive range of diseases. As a full-service CRO with labs, imaging, a phase I unit, and cardiac safety capabilities, we offer comprehensive services and the support of our collective expertise to accelerate your studies and programs.
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