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Biometrics
GENERAL CAPABILITIES

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Medpace is ready to help you with your next clinical trial project. Find out more about how we can help.

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Advancing your drug to regulatory approval in the most efficient and cost-effective manner requires a concentrated effort every step of the way. The right data demands the right people with the right knowledge in the right parts of the world.

Led by scientific and technical experts, the Medpace Biometrics team has the clinical data management and statistical expertise to consistently deliver high-quality data that accelerates your clinical development process. Involved at every phase of drug development – from study design to delivery of the Integrated Clinical Statistical Report – our highly-qualified team of specialized statisticians, programmers, and medical writers have a better understanding of data supporting our therapeutic areas of expertise.

Our global standard operating procedures (SOPs), combined with continuous quality control, ensure consistent, efficient, and comprehensive data that meet all Sponsor protocol requirements. All clinical data is integrated into Medpace's state-of-the-art, validated, and 21 CFR Part 11-compliant suite of proprietary technologies, ClinTrak®, a study management system facilitating team coordination and providing decision support for sponsors and sites to ensure global teams are focused and organized for maximum efficiencies using a common data platform. ClinTrak provides near real time access to clinical data and study metrics pertaining to the study.

Delivering high quality data management, superior statistics, and expert report writing, we are responsive, flexible, and knowledgeable in our approach so you can have complete confidence in your data for the entire duration of drug development. We undertake each study with one goal in mind – correctly preparing your statistical data for submission, on time and on budget.

Data Management – Our data management team provides high-quality collection, organization, validation, analysis, and quality control of clinical trial data and utilizes electronic data capture (EDC) to expedite data collection.

Biostatistics – Our skilled group of biostatisticians provides statistical programming and analysis to create a customized approach designed specifically to meet your project requirements.

Want to learn more? Browse our capabilities, or contact the location nearest you.