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Clinical Services

CTI offers the full spectrum of clinical trial services with a proactive and integrated approach.  Our team of operations experts averages more than 15 years of clinical trial and/or patient management experience.

Start-up Services

When CTI manages study start-up tasks, total start-up time is generally less than half the industry average.

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Project Management

Our experienced global project managers are highly committed to their projects and are dedicated to providing quality services.

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Clinical Monitoring

With an average retention rate of over 94% over the last five years, and decades of industry experience in critical patient populations, our CRAs are able to see their studies through from start-up to close-out.

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Medical Monitoring

CTI’s Medical Affairs team has extensive clinical, academic, and Phase I-IV clinical trial experience, in addition to decades of experience in the industry.

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Safety & Pharmacovigilance

CTI’s global Safety and Pharmacovigilance team has broad experience with a variety of databases and technology, in addition to concentrated experience with critically ill patients.

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Clinical Data Management

CTI's Data Management team provides guidance to sponsors on the most appropriate method of data collection to best serve the needs of the study sites and project team.

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Biostatistics

Our biostatisticians are involved in the entire lifecycle of drug development from regulatory pathway design through medical writing.

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Regulatory Affairs

Our Global Regulatory Affairs department is experienced in assisting sites around the world with local and central Institutional Review Board (IRB)/Ethics Committee (EC) submissions.

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Quality Assurance

Our independent Quality Assurance team has decades of industry experience, and performs audits of internal systems and processes, departments, and study related services and procedures.

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Late Phase & Expanded Access Programs

CTI has the global infrastructure, site relationships, and health outcomes expertise to execute Phase IV, Registry, and Expanded Access Programs (EAPs) effectively.

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Health Resource Data Collection Within Clinical Trials

CTI's HECOR team helps our sponsors evaluate the best way to collect health resource utilization data, whether it is within a randomized controlled trial or through a pragmatic clinical trial.

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