Coderant specializes in providing custom clinical data management services. Coderant’s methodical approach to system design and management, ensures the predictability and robustness that the FDA requires throughout the clinical trial process.

Coderant begins by understanding each unique study design and objective. This is done through a series of medical reviews performed by Coderant’s staff of physicians, scientists and regulatory personnel. This review often yields the template for a comprehensive case report form which forms the backbone for all of Coderant’s clinical data management offerings.

With a clear understanding of the trial, Coderant builds a layered database built on leading database platforms such as Oracle, MSSQL and Sybase. The database is then customized to incorporate each sponsor’s reporting requirements and logistical constraints.

Finally, Coderant provides clinical data management services to connect the sponsor and the trial participant though validated data transfer. These services include medical monitoring, clinical data entry and statistical modeling.