New Therapies by Designing and Implementing Multiple Phases of Human Clinical Trials
Medical research is a continuum that begins with a promising concept and concludes with proving the safety and efficacy of a new therapy in a controlled clinical trial. CRF's Clinical Trials Center provides comprehensive and complete trial design, evaluation, and analysis services.
The Clinical Trials Center (CTC) sets the standard for conducting clinical research, offering a full spectrum of interventional and pharmacological evaluations with unmatched expertise. The CTC combines the comprehensive knowledge of leading physicians and technologists to streamline the research process from Phase I through Phase IV trials.
Operating as a full-service academic research organization, the CTC plans and executes clinical investigations, from first-in-man studies to multicenter trials, and provides independent qualitative and quantitative analyses of clinical and imaging data. With more than 20 years of experience in cardiovascular clinical trials, the CTC can standardize the way data is collected, evaluated, and disseminated around the world, making it easier to pool and analyze. In short, the CTC is making clinical research far more convenient for trial sponsors while maximizing the quality of the data in the most time- and cost-efficient ways possible.
The CTC provides the full spectrum of services needed for successful clinical research, including clinical and regulatory strategy, protocol and database development, statistical analysis, safety surveillance, and core laboratory capabilities. This full portfolio of abilities means our clients can have a tailored research plan that meets their needs.
