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Global clinical development experience
Therapeutic, global experience to support all phases of clinical research


Find out how our clinical research expertise in drug and medical device can help with your next study or program.


GENERAL CAPABILITIES



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PDF: Medpace Fact Sheet

EXPERIENCE brings efficiencies to your clinical development


When you work with Medpace, you benefit from over 20 years of therapeutic excellence in Phase I-IV global clinical research. Sponsors developing drugs and medical devices that match Medpace's core therapeutic and specialty areas will find exceptional depth of resources and experience. These include:

Therapeutic Strengths
Cardiovascular Metabolic
Oncology Infectious Disease
Neuroscience Nephrology

Specialties
Regenerative Medicine Pediatrics
Rare/Orphan Diseases

Global Phase I-IV Experience

Medpace has the global reach and resources to conduct studies in drugs, biologics and medical devices. Our in-house experts work collaboratively to support your entire product development lifecycle. We provide a full range of services to advance your compounds and medical devices from early clinical development through late phase studies.
  • Phase I/IIa: Medpace can help assess safety, identify risks, and set a course for successful development at this critical early stage.
  • Phase II-III: Medpace provides scientific leadership with disciplined execution, global access to patients, and local and global regulatory expertise
  • Phase IIIb-IV: Extending our integrated model and expert teams into late phase, Medpace conducts both interventional and non-interventional type studies to address safety and efficacy, outcome decisions, risk management, and post-marketing commitments

Drug - Device Combination Experience

Drug-device combination products can present unique considerations and risks. With a dedicated Medical Device division, Medpace brings together its medical and regulatory experts into a collaborative team that understands the nuances from both the drug and device perspectives. Medpace is experienced in helping clients meet regulatory compliance and ensuring patient safety while accelerating their combination product to market.



Discover the Power of X in Clinical Research and how Medpace can accelerate your drug and device development with our powerful combination of: