Decentralized Clinical Trial Services

Our Services

  • 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.
  • Remoting Monitor

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

    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.
  • 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.

Central Site

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.

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