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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Established in 1992, Medpace partners with leading pharmaceutical, biotechnology, and medical device companies to bring promising new drugs to market. As a full-service Clinical Research Organization (CRO), we combine efficient clinical trial management, comprehensive regulatory consulting, and innovative technologies to create a customized approach that ensures powerful solutions for our partners around the globe.

Led by therapeutic experts with extensive experience in the advancement of pharmaceutical agents for use in multiple therapeutic specialties, Medpace's dedicated teams deliver rapid and accurate clinical trial results for the most complete Phase I-IV clinical research support in the industry. Our regulatory experts; former government officials with valuable international insight into specific areas of drug approval are involved at project initiation, allowing them to develop an accurate description of your data to ensure that every phase of trial is precisely focused for maximum results.

Regardless of project size, Medpace has the breadth, depth, experience, and flexibility to deploy a study on six continents.

Our full-range of integrated and customized services includes:

• Clinical Operations – including regulatory submissions, investigator selection, clinical monitoring, and clinical trial management.
• Medical Writing & Reviewing – including Marketing Approval Applications and New Drug Applications (NDA).
• Biometrics – including Data Management, Electronic Data Capture (EDC), and Biostatistics.
• Regulatory Support – including protocol planning and strategic development plans.
• Quality Assurance – including validation compliance and auditing.
• Pharmacovigilance – comprehensive identification and assessment of risk during clinical trials.
• Interactive Voice Response System (IVRS) – our proprietary system is web and phone interchangeable.
• Medpace Reference Laboratories (MRL) – a state-of-the-art, full-service, central laboratory providing Phase I/IIa confined and controlled clinical studies.
• Medpace Bioanalytical Laboratories – obtain accurate, high-quality results with complete bioanalytical laboratory services.
• Medpace Cardiovascular Core Laboratory – state-of-the art, ECG technologies and centralized electrocardiography data analysis to support Phase I-IV clinical trials.
• Medpace Imaging Core Lab – a centralized imaging core laboratory.
• Medpace Clinical Pharmacology (CPU) – a state-of-the-art recruitment and diagnostic facility.
• Pharmacokinetics & Pharmacodynamics – complete analysis of drug concentration and drug response.

Want to learn more? Contact the location nearest you.