Medpace
Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpaces mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach that leverages local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs approximately 2,600 people across 36 countries.
Solutions
Throughout the development life cycle, Medpace provides medical and regulatory leadership and guidance, with efficient, disciplined operational execution of your studies around the world. We can conduct studies in any phase:
- Early Phase: Strategies, services, and execution to accelerate Phase I clinical development from first-in-human to proof-of-concept.
- Phase II-III: End-to-end collaboration and comprehensive services to support global research and the advancement of life-saving therapeutics.
- Late Phase: Bridging the gap from development to commercialization with real world evidence (RWE) and late phase clinical research.
Medpace Medical Device is a specialized entity dedicated to developing medical devices, drug-device combinations, and diagnostic trials. Our medical, regulatory and operational experts work collaboratively with your team to design and conduct clinical research trials around the world.
Capabilities
Driven by a full-service CRO model that coordinates and integrates all services for our clients, Medpace provides an accountable, seamless, integrated platform for executing clinical research increasing quality and speed while reducing the need for duplicate management oversight. Our disciplined processes, site relationships, and technologies enable us to execute even the most complex global studies.
- Medical Affairs: Physicians provide hands-on leadership to design, monitor, and execute your programs.
- Regulatory Affairs and Medical Writing: Global leadership and a holistic approach guides your program forward.
- Clinical Monitoring: Quality oversight from highly-trained teams.
- Clinical Trial Management: Disciplined recruitment, study start-up and trial execution
- Biometrics & Data Sciences: Data management and biostatistics to accelerate the clinical development process.
- Safety & Pharmacovigilance: Comprehensive suite of pharmacovigilance services.
- Quality Assurance: Independent assessment of regulated research to minimize risk and prevent errors that matter.
- Technology: Study Management System Using a Common Data Platform
Laboratories
Medpace Central Laboratories delivers key support for fully integrated studies on a global stage by providing consistency in methods and instrumentation across wholly owned and purpose built laboratories around the world. Medpace Central Laboratories has provided core laboratory support to trial sites with truly stellar performance.
Medpace Bioanalytical Laboratories has significant experience working with small molecules, biologics, and biomarkers across a wide variety of technologies and therapeutic areas. Our experience spans chromatography, mass spectrometry, ligand binding assays, cell-based assays, and flow cytometry. Medpace Bioanalytical Laboratories is a leading provider of bioanalytical services in all stages of drug development from discovery to post-marketing.
Medpace Core labs houses our Imaging Core Labs proving an end-to-end suite of global imaging services to enhance and expedite biopharmaceutical and medical device development, and our cardiovascular Core Labs providing standardized electrocardiogram (ECG) equipment to support Phase I-IV clinical trials around the world.
Medpace 5375 Medpace Way, Cincinnati, Ohio, 45227
+1.513.579.9911
