At the end of your trial, the CANTAB data are typically analysed in an interpretive report, putting the results into context and drawing comparisons with the literature.

The interpretive report for your clinical trial will be written by one of our external consultants, who are each experts in the CANTAB tests, their application, and neuropsychopharmacology. We work with you to meet the requirements for your clinical study report, and have a documented process for the provision of reports to ensure a timely and accurate conclusion to your trial.