Experts in Protocol Design, Data Management, Core Laboratories, Clinical Events Adjudication, and Regulatory Support
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. The CRF Clinical Trials Center provides comprehensive and complete trial design, evaluation, and analysis services.
The CRF Clinical Trials Center (CTC) is a full-service academic research organization, providing expert thought leadership, comprehensive trial design, evaluation, and analysis services. 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 makes clinical research 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.
Specializing in:
CRFiCOR
- Angiography (Coronary, Peripheral, Structural, Physiology)
- Intravascular Imaging
- Noninvasive Imaging
- Electrocardiography
- PCI Appropriateness Evaluation
Data Safety
- Event Adjudication
- Data Monitoring Committee
Biometrics
- Data Management
- Programming
- Statistics
- Medical Writing
- Research Office
For more information, please contact:
Business Development
CRF Clinical Trials Center
Tel: 646-434-4136
E-mail:
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