ClinPro, Inc. is a growing, independent, full service clinical research organization (CRO) offering veteran clinical researchers with expertise in a variety of therapeutic areas.

We base our success on our people, processes, technology and our ability to treat each customer as if they were our
only one.

We provide our sponsors with the full suite of clinical trial capabilities of a big-name CRO with the dedication of a small firm. From study design through clinical trial and data management, to statistical services and regulatory submissions, ClinPro's size and focus enable us to provide our clients with results - on time and within budget.

We provide our clients with the most qualified team for designing, implementing and executing their clinical development programs. ClinPro's senior management team brings years of clinical research experience in the pharmaceutical and biotech industries, in academia and in the pharmaceutical outsourcing business. Our experienced staff of project managers, Medical Research Associates (MRAs), physicians, programmers, statisticians, data managers, and site managers is highly trained in standard operating procedures (SOPs) and Good Clinical Practices (GCPs).

We utilize the latest technologies for project management, communications, data management and FDA submissions. ClinPro manages timelines for clinical studies using the suite of ClinPlus data management and reporting software, as well as with our proprietary project management system, ClinOps. Through the Internet and email, we continually communicate the program's progress and status to the sponsor team.

We have a database of investigators and a wealth of experience in managing clinical trials across numerous specialties. With years of clinical trial management experience, the ClinPro team has therapeutic expertise in oncology, infectious disease, cardiology, respiratory care, endocrinology, central nervous system (CNS), ophthalmology, medical devices and primary care. Within each therapeutic specialty we work with physician experts to design protocols that meet the clinical and regulatory needs of our sponsors. The ClinPro team manages studies to deliver your data with quality, efficiency and timeliness, in order to speed the drug development process.

Partner with a Proven Leader

ClinPro Inc. is a full-service clinical research organization providing comprehensive clinical trial management services for Phase I, II, III IIIb and IV clinical trials. The company uses fully validated, proprietary project management and data management systems for managing clinical trials combined with cutting-edge communications tools and a highly customizable approach to service to meet each client's budget and timeline. Our complete range of services include site management and monitoring, data management, biostatistics, health economics, regulatory services, and medical communications and meeting management. Highly trained management team and cutting-edge technology distinguishes ClinPro from the competition, the combination of which provides clients with an unparalleled level professionalism and flexibility in the CRO field.