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As an IRT (IVRS/IWRS) specialist, we understand the importance of access to real time, accurate data throughout the duration of your clinical trial. Our versatile reporting module utilizes SAP Business Objects, a class-leading Business Intelligence Solution. You’re in control as you leverage sophisticated, easy-to-use reporting dashboards. And you can increase specificity by drilling down through the data to the precise information you need. Our system is flexible, so we can implement tailored reports for any study.

Flexible access to reports

You will be able to access and export all reports from the web (PDF and Excel) in real time, 24 hours a day, 7 days a week. You can also have reports delivered as an email attachment on a defined schedule or triggered by an event in the IRT system.

Sponsor users, including monitors/CRAs, have access to reports available for the study. However, it is possible to limit report access to some users based on their role and blinded status in the clinical trial.

For example:

  • Drug safety may have access to a treatment group unblinding report
  • The clinical materials manager may have access to a treatment group unblinding report
  • The clinical trial materials manager will have access to unblinded site or warehouse inventory reports
The reporting tool can also allow sponsors to provide reports filtered for a specific site to investigators.