SFS provides an electronic case report form which complies the FDA requisites (21 CFR Part 11) and has a user-friendly interface attractive for PIs and Sponsors. The accumulated experience in this field allows SFS to create customized platforms in a very short term, including query management, adverse event inclusion and report generation.

We program
and create the eCRF.

We train
the sites and principal investigators previously to the beginning of the data entry phase.

We improve
continuously the interface for PIs, monitors and sponsors.

We generate
online and by demand reports.