SAE Reporting

Get Clincase involved. We offer powerful, robust features, services and add-on modules that scale to fit and streamline your data and your clinical trials.

Stay focused with Clincase’s SAE (serious adverse events) Reporting Module. This module is essential for those who need to stay one step ahead of their clinical trial data. Clincase provides enhanced functionality for SAE email notifications that notify data managers and other important players involved in your study’s drug safety efforts. Notifications can include a printout of the data of the SAE and associated forms.

Use Clincase’s SAE Reporting Module to ensure that you are meeting regulatory requirements and to promote the progress of your clinical trials. This supplemental module is an essential add-on to your EDC and clinical data management strategy.

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