Our Full-Service Model
A Message From Our CEO & Founder
“To our current and future Sponsors –
Since 1992, Medpace has steadfastly held to a model of providing full-service clinical development to biopharmaceutical and medical device Sponsors. Even as the industry continues to explore various outsourcing/insourcing models – functional, clinical staffing and hybrids – Medpace chooses to drive success for Sponsors through full-service clinical trial outsourcing.
We know from our long-standing relationships with Sponsors that the full-service outsourcing model ultimately delivers higher quality results.
When we can fully engage with our medical, regulatory and operational teams and work under our SOPs, we can perform at the highest levels to deliver quality results in the most timely and efficient manner. 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.
I share my philosophy on full-service outsourcing with you because it has stood the test of time. I truly believe it is the best path for our Sponsors.”
– August Troendle, MD
Medpace Founder and CEO since 1992
Our Integrated Approach
Purpose-Built Technology
ClinTrak® is a proprietary, feature-rich, and fully customizable Clinical Trial Management System to inform decision making, drive efficiencies and keep your study on track.
Clinical development projects require a common data platform to facilitate team coordination and provide decision support for sponsors and sites – ensuring global teams are focused and organized for maximum efficiencies. Making the wrong decision based on poor quality data is a main reason studies fail.
Choosing the right development partner with an integrated, robust technology platform is a critical step for ensuring successful studies are conducted at the highest level of data integrity.
Full Service Verses Functional
Our operating model was designed to accommodate efficient partnering with emerging biopharma companies.
Full-Service CRO
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.
Clinical Trial Management System
Clinical development projects require a common data platform to facilitate team coordination and provide decision support for Sponsors and sites – ensuring global teams are focused and organized for maximum efficiencies. Making the wrong decision-making based on poor quality data is a main reason studies fail.
Choosing the right development partner with an integrated, robust technology platform is a critical step for ensuring successful studies are conducted at the highest level of data integrity.
