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Curavit’s digitally enabled clinical site platform collects each participants electronic health information, leverages telehealth solutions, and fully integrates with the leading clinical trial decentralized software solutions, ensuring our clients realize all the advantages of their software investments.

For each new trial, Curavit assigns an experienced principal investigator (PI), who is an expert in the specific disease area under study, to engage with the protocol development and regulatory submission process.  

Once the study kicks off, Curavit manages participant recruitment and enrollment, and, under the direction of the PI, Curavit’s clinical study team executes the entire clinical trial.  

Curavit’s site is always audit ready and supports remote monitoring.