Medpace, Inc.
Medpace is a global contract research organization (CRO) dedicated to accelerating the development of safe and effective medical therapeutics. With over 30 years of experience, Medpace offers a full-service, integrated approach to clinical research, emphasizing quality, scientific expertise, and operational excellence. The company supports a broad range of therapeutic areas, provides comprehensive laboratory and imaging services, and maintains a strong global presence to reach diverse patient populations. Medpace's mission is to make the complex seamless in clinical development, ensuring high-quality results and fostering innovation in healthcare.
Industries
Nr. of Employees
Very Large (1000+)
Medpace, Inc.
Products
Proprietary clinical trial management and electronic data capture platform
Integrated CTMS and EDC platform used to manage study operations, IRT, eTMF, centralized monitoring and study-specific data flows.
Patient-facing trial engagement mobile application
Mobile application for patient engagement, ePRO/eCOA data capture, and remote data collection from wearables and diaries.
Site-facing trial management mobile application
Mobile application for site staff to manage visits, data capture touchpoints, and site communications with sponsor/CRO systems.
Proprietary clinical trial management and electronic data capture platform
Integrated CTMS and EDC platform used to manage study operations, IRT, eTMF, centralized monitoring and study-specific data flows.
Patient-facing trial engagement mobile application
Mobile application for patient engagement, ePRO/eCOA data capture, and remote data collection from wearables and diaries.
Site-facing trial management mobile application
Mobile application for site staff to manage visits, data capture touchpoints, and site communications with sponsor/CRO systems.
Services
End-to-end outsourcing of clinical development programs, including study strategy, start-up, monitoring, clinical trial management, vendor oversight, and program-level account management.
Centralized sample processing, safety testing, biomarker assays, and biorepository management to support clinical trials.
Quantitative bioanalytical support for discovery through post-marketing, including PK/TK studies, biomarker methods, ADA and neutralizing antibody assays.
Centralized imaging management, image quantification, and ECG/cardiac safety services to collect and analyze imaging and cardiac endpoints.
Clinical pharmacology unit services for first-in-human, SAD/MAD, DDI, food-effect, TQT/QTc, and other early-phase designs with inpatient/outpatient capability and licensed investigational drug services pharmacy.
Regulatory strategy, dossier preparation, protocol and submission writing, and consulting to support regulatory interactions and filings.
End-to-end outsourcing of clinical development programs, including study strategy, start-up, monitoring, clinical trial management, vendor oversight, and program-level account management.
Centralized sample processing, safety testing, biomarker assays, and biorepository management to support clinical trials.
Quantitative bioanalytical support for discovery through post-marketing, including PK/TK studies, biomarker methods, ADA and neutralizing antibody assays.
Centralized imaging management, image quantification, and ECG/cardiac safety services to collect and analyze imaging and cardiac endpoints.
Clinical pharmacology unit services for first-in-human, SAD/MAD, DDI, food-effect, TQT/QTc, and other early-phase designs with inpatient/outpatient capability and licensed investigational drug services pharmacy.
Regulatory strategy, dossier preparation, protocol and submission writing, and consulting to support regulatory interactions and filings.
Expertise Areas
- Integrated clinical trial management
- Early-phase clinical pharmacology and FIH studies
- Central laboratory and bioanalytical testing
- Imaging and cardiac safety core labs
Key Technologies
- Electronic data capture (EDC)
- Clinical trial management system (CTMS)
- Interactive response technology (IRT)
- ePRO / eCOA / eConsent