Making the Complex Seamless
We can’t simplify clinical development – but we can execute it seamlessly
THERAPEUTIC FOCUS
Scientific expertise embedded in trials – hands-on and specialized
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.
INTEGRATED EFFICIENCY
A model of collaboration – an end-to-end partner
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.
“Competence and empowerment to coordinate all services under one roof provides an accountable, seamless, integrated and efficient platform – increasing quality and speed while significantly reducing a Sponsor’s need for duplicate management oversight.”
August Troendle, MD, Medpace Founder and CEO since 1992
GLOBAL REACH
Operational around the world – wherever research is happening
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.
ORGANIC GROWTH
Stable and disciplined – preserving a culture of quality
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 other 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.
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.
