We have implemented efficient study monitoring methods based on ongoing data review, and ongoing communication with sites to address issues as they arise, so to minimize protocol deviations.

Close collaboration with core labs allows us to ensure that study data are generated per protocol and on time. Our goal is to maintain sites audit ready at all time, and the discrepant data queried on an ongoing basis.

The resulting benefit of such close attention is an extremely reduced time from study (milestone) completion to data (interim) analysis and clinical study report.