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At SYNARC, we distinguish ourselves by providing superior accuracy, precision, and speed in central image analysis for clinical trials.

In addition to having the broadest and deepest expertise available, our scientists helped pioneer many of the methods used in trials today. We are committed to collaborating closely with leading universities, government agencies, and research foundations to identify and implement innovative imaging techniques that accelerate therapeutic development. When you need reliable medical imaging for your development program, contact SYNARC.

Highly accurate assessments of efficacy and safety

SYNARC medical-imaging services are designed to reduce the variability inherent in multisite, international clinical trials, thereby maximizing the accuracy of efficacy and safety imaging assessments. Because of our extensive experience and technical knowledge, we are able to design study protocols that accommodate the diversity in imaging infrastructure that exists across the sites in a clinical trial. This optimizes the consistency and quality of the images produced and the accuracy and precision of the image analyses performed by our specialized in-house radiologists.

 

 

Rapid Results

At SYNARC, our imaging techniques have the industry’s highest discriminative power and sensitivity to change. As a result, our trials require fewer subjects and therefore less time in the recruitment phase. SYNARC also provides rapid image processing, image analysis, and data delivery.

Trusted scientific and regulatory experts

SYNARC medical and scientific experts are luminaries in their fields, and have authored thousands of peer-reviewed articles and served on numerous international scientific, regulatory, and industry panels. Under their guidance, your image data are collected and analyzed according to the highest and most current standards.

 

Link to SYNARC medical imaging devision 

 

 

Benefits of the CCBR Model

  • Working with CCBR speeds up and drives efficiencies in clinical trials by offering greater numbers of patients across fewer sites

  • A Global Footprint covering more than 20 dedicated Clinical Research Centers in high density population areas

  • Uniform SOPs enable the tightest possible adherence to study protocols and consistency across all CCBR sites

  • Real-Time tacking of subject enrolment and trial progress ensures sponsors have the most up to date information, all of the time

  • Centralised, standardised billing affords better visibility into trial costs for sponsors

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