The best in class IRT solution

S-CLINICA’s multilingual IRT (IVRS/IWRS) is a robust and highly customizable solution that supports central randomization and drug supply management in global clinical trials. IRT is not only for central randomization and drug assignment! To facilitate decision-making and monitoring of the trial, our system offers numerous reporting and trial management options. It allows controlling and managing clinical trials in real-time.

We can help you analyze the project challenges and manage them in the most efficient way.

Key Features

  • Unique study set up of the IRT
  • Simple management of any study design (including adaptive trials)
  • Central randomization of patients
    • Any randomization method (permuted blocs or dynamic)
    • Eligibility control
  • Treatment assignment to patients
    • Multiple treatment assignment to a patient
    • Dose adjustments
  • Event/visit tracking
  • Emergency unblinding
  • Specific study management and patient recruitment options (center cap, cohort management, screening slot reservation with queue)
  • Unique drug supply management
  • Full integration with S-CLINICA’s eCRF
  • Real time data transfer & data integration
  • Localised language access, any language available upon request
  • Real-time web reporting (including downloadable reports)
  • Automatic customized report sending via e-mail
  • 24/7 Helpdesk

Key Benefits

  • Reduced risk, timelines and cost
  • 100% flexibility of the system allows simple management of complex and adaptive clinical trials
  • Real-time study management