Fullcro is able to manage all processes in a Clinical Study, from the drafting of protocol to publish data

  • Clinical Operations
  • Start-up
  • Set-up
  • Project Management
  • Clinical Monitoring
  • Data Management
  • Safety
  • Quality Assurance
  • IT Support
  • Statistics
  • Medical Writing

Focus on

  • Knowledge of the centres’ potential – collaborative approach – study team loyalty
  • Speeding up the authorization process of the study
  • Achieving high enrolment target in a short time
  • High experience in the use of computing devices for administration of questionnaires to the patient
  • Knowledge and management of the issues and real time resolutions

Dedicated Platform to Remote Monitoring

Solution in addition to the traditional monitoring, to contain the conduct of the trial costs and optimizing the intervention time.

Application and TMF

The Electronic Trial Master File makes possible to control and easily sync the study files, to track the advances of the study, to assure fast and sure access to documents before, during and after the study.

“No-Profit”  Study

Optimized solutions to support no-commercial promoters in all phases of the study. Document management and the relationship between dispenser funding, promoter and CRO.
Contract proposal tailored with respect to the type of the study.