Our centralized clinical trial data management environment provides a compliant and standardized methodology for processing, validating and presenting real-time information to clinical trial managers and monitors.

Our processes have been finely tuned to ensure quality work in a timely manner:

• Provide quality solutions for the entire clinical data process, from initial CRF to submission, which can be customized to fit each client specific needs
• Reduce costs by transforming "traditional" monitoring tasks through technologies
• Accelerate timelines through the use of proprietary tools for more rapid data collection that can be used by sites and patients for direct entry into study databases

From thought to finish, i-clinics provides timely and accurate clinical trial data at every phase of development allowing you to make sound and cost-efficient decisions about safety, tolerability, efficacy, and marketability for your product.