One CRO Providing Consistent Execution
Partnering with a global medical device CRO that fully understands how to navigate and accelerate clinical research and approvals around the world means your timelines and budgets will be managed as efficiently as possible. With dedicated device teams in the U.S. and Europe, Medpace Medical Device has the global scope to provide a comprehensive array of services to support the needs of your trial.
A Global Partner That Understands Your Needs
Our global presence and experience means more than just having feet on the ground. Our geographically diverse and multilingual employees understand the local cultural environment for clinical research and your regulatory pathway:
- Established relationships with clinical research sites, key opinion leaders and therapeutic networks experienced in medical device trials allows Medpace to select the ideal geographies and sites to ensure key milestones are met
- Regulatory affairs staff provide guidance in selecting the optimal regulatory pathway and have the experience to coordinate and lead meetings with FDA and EU notified bodies
- Multilingual staff ensure your program is interpreted and implemented efficiently and appropriately
- Physician-led model provides therapeutic and scientific leadership throughout your program’s lifecycle