Curavit utilizes digital consent and enrollment of subjects embedded in its platform.Consent & Enrollment
Curavit coordinates all of the complex logistics required to run a fully decentralized trial.Direct-to-Patient Logistics
Curavit’s central site supports 100% remote based monitoring.Remoting Monitor
Curavit clinical study teams monitor the trial data in real time to ensure patient safety, protocol adherence and patient retention. incorporates digital consent, telehealth, and remote data capture technologies.Clinical Oversite
Curavit data management team will create the statistical plan and provide full data analysis for the final study report.Data & Intelligence
Curavit will manage the central IRB and other necessary regulatory requirements.Regulatory
Curavit works with world-class principal investigators, to identify endpoints and create protocols from “first principles”, to design studies that are digitally native.Study Design
Through social channels and electronic health records, Curavit recruits participants from the 97% of potential participants who are traditionally excluded from clinical research, including ethnically and socio-economically underserved and underrepresented populations.Patient Recruitment
Decentralized Clinical Trial Services
Our Services
Curavit's Decentralized Clinical Trial Services
Central Site
Curavit has a fully virtual, always audit-ready “site” to conduct decentralized clinical trials, with a purpose-built clinical platform that manages the critical CRO and Site requirements and integrates with all leading clinical applications.
Study Design
Curavit works with world-class principal investigators, to identify endpoints and create protocols from “first principles”, to design studies that are
digitally native.
Patient Recruitment
Through social channels and electronic health records, Curavit recruits participants from the 97% of potential participants who are traditionally excluded from clinical research, including ethnically and socio-economically underserved and underrepresented populations.
Consent & Enrollment
Curavit utilizes digital consent and enrollment of subjects embedded in
its platform.
Direct-to-patient Logistics
Curavit coordinates all of the complex logistics required to run a fully decentralized trial.
Remote monitoring
CCuravit’s central site supports 100% remote based monitoring.
Clinical oversight
Curavit clinical study teams monitor the trial data in real time to ensure patient safety, protocol adherence and patient retention. incorporates digital consent, telehealth, and remote data
capture technologies.
Data & Intelligence
Curavit data management team will create the statistical plan and provide full data analysis for the final
study report.
Regulatory
Curavit will manage the central IRB and other necessary regulatory requirements.
