The system offers advanced search functionality that allows personalized searches across various fields. This enables quick identification of desired clinical studies and obtaining an accurate overview of the data.
For each clinical study, it is possible to track all administrative activities, adverse event reports (SAEs), amendments, and recruited patients. This allows monitoring the progress and progression of each study or conducting more general analysis.
The system gathers all administrative information for each clinical study, including protocols, drugs, study types, sponsors, involved facilities, lead researchers, departments, and all other relevant data such as study start and end dates, ethical committee and regulatory approval, and different study phases.
The system allows uploading document templates to facilitate automatic creation of study management documentation. Templates can be customized.
The system allows exporting reports with all the information regarding individual clinical studies or an entire set of studies. These reports provide detailed analysis of aggregated data and trends in ongoing clinical studies. Reports can be customized according to specific needs.
The system supports different permissions and access levels for users. Specific roles and appropriate permissions can be assigned to each user, ensuring they only have access to relevant functionalities and data for their role.
Designed to accommodate the evolving needs of organizations handling multiple trials. It can integrate with regulatory submission platforms allowing for direct transfer of trial documents.
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