Designed to minimize risks, ensure strict adherence to study requirements and timelines, and safeguard trial integrity by swiftly identifying and addressing deviations or issues.

Enables to have real-time information about drug supply at the sites, issuing automatic alerts to inform users and vendors about the immediate actions required.

Allows casual assignment a specific treatment, ensuring that participants are assigned to different groups receiving various treatments by chance.

It facilitates the import of data into the study database and allows for export in various formats such as XLS, CSV, thereby simplifying data management for the team and providing convenient access to individual study participants.

Enables tailored training for all investigators participating in a clinical trial, not only for the trial protocol but also for the use of the system itself.

Allows investigators to access all safety information in a single container. Expedites the procedures for sending, reporting events, with a highly adaptable solution for SAE or pregnancy notification reporting.

Enables to make the trial more subject-friendly, limiting visits to the hospital & clinic creating a direct connection between the subject and the study staff that is easy to access.

Permits to capture a complete view of patient well-being through our comprehensive archiving system, accommodating everything from daily smartwatch snapshots to intricate images like X-rays and CT scans.

Empowers customers to tailor their tool to their specific needs while relying on OPIS Staff for more technically complex aspects of the clinical trial process.

Manages the pre-allocation of subjects who could be enrolled in different trial phases, matching patients to the most cost-effective level of care and the most clinically appropriate one.

Strictly related to the patient allocation in a study, allowing the Sponsor to modify dose assignments and the users to kept update via email notifications.

Cell and gene therapy (CGT) is an innovative approach to treating various diseases by harnessing the power of cells and genes to address underlying genetic or cellular defects.