Making the Complex Seamless
We can’t simplify clinical development – but we can execute it seamlessly
Quality at our core
Built to execute – enabled by organic growth
Accelerate your clinical development by partnering with a CRO that is structured to keep study teams focused on execution. This commitment to quality extends to the projects we engage in – we are selective to ensure we deliver the highest levels of service and partnering. Our unique approach has been preserved by 30+ years of organic growth – delivering consistency and stability while avoiding the disruptions associated with mergers and acquisitions.
Team Continuity
Expertise embedded in trials – throughout the project lifecycle
Engage with one cross-functional team that actively participates in your trial or program – from early planning through close-out. Our approach maintains continuity and optimizes performance while building strong team chemistry, minimizing disruptions, and ensuring high-quality results across our full breadth of services. With deep scientific and therapeutic expertise, our teams are poised to lead the industry’s most innovative and challenging clinical trials.
Integrated Services
End-to-end partnership – a model of productivity
Streamline even the most complex clinical trials with a full-service, single-vendor outsourcing strategy. Our comprehensive CRO services are supported by our wholly-owned Central Laboratories, Bioanalytical Lab, Imaging Core Lab, ECG Core Lab, and Phase I Unit, as well as a Clinical Trial Management System that ties all study data together in a single platform. With integrated services and systems, we achieve higher levels of efficiency and productivity.
GLOBAL Engagement
Navigating cultures and requirements – reaching patients around the world
Leverage our country-specific experience and breadth of in-house expertise to navigate languages, cultures, and clinical and regulatory environments around the globe. Our resources extend across North America, Europe, Latin America, and Asia Pacific with strong site and Investigator relationships to reach targeted and diverse patient populations. Our global reach and experience across all phases of development and key therapeutic areas can help streamline your clinical trials and reach your development goals faster.
Testimonial: Why Medpace is Trusted by Biotech®
The Medpace Advantage
A Full-Service Model for Quality and Efficiency
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®.
Therapeutic Areas
Embedded Therapeutic Expertise
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.
CRO Capabilities
Our One Team Approach
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.
Lab Capabilities
Global Labs –
Fully Integrated for Efficiency
Because almost every clinical trial requires laboratory support, having wholly-owned entities with a broad range of capabilities and comprehensive test menus provides built-in efficiencies and collaboration. In concert with the Medpace CRO or working on standalone projects, experts from our central laboratories and bioanalytical laboratory can help plan and execute your testing needs.
DEI in Clinical Trials
A collaborative approach – Sponsors, Medpace, and Sites working together to achieve diversity, equity, and inclusion in clinical trials.
Decentralized Clinical Trials
A customized approach – incorporating DCT capabilities to tailor a best-fit trial design to your program’s objectives and position your trial for success.
Remote Biosensing Technologies
Enabling the continuous collection and real-time transmission of patient biomarker data to provide vital operational and analytical advantages.
