Curavit Clinical Research services

Curavit coordinates all of the complex logistics required to run a fully decentralized trial.

Curavit utilizes digital consent and enrollment of subjects embedded in
its platform.

Curavit works with world-class principal investigators, to identify endpoints and create protocols from “first principles”, to design studies that are
digitally native.

Curavit will manage the central IRB and other necessary regulatory requirements.

Curavit’s central site supports 100% remote based monitoring.

Curavit data management team will create the statistical plan and provide full data analysis for the final
study report.