Vijio - Turkish Pharmacovigilance Master-AI-powered Pharmacovigilance

Example

When a pharmaceutical company identifies a new adverse reaction during a clinical trial, Vijio assists in filling out the TÜFAM form by prompting the user for specific, necessary information such as patient demographics, description of the adverse event, and the suspected medication.

Scenario

A user is notified of an adverse event. Using Vijio, the user logs into the platform and selects the 'New Report' option. The system provides a step-by-step guide to input all required data, ensuring completeness and regulatory compliance.

Example

Vijio includes a comprehensive database of regulatory requirements and updates related to pharmacovigilance in Turkey. It can alert users to changes in legislation or new reporting requirements.

Scenario

A regulatory change is announced by the Turkish Medicines and Medical Devices Agency. Vijio updates its guidance accordingly and notifies users through an alert system, ensuring that they are always compliant with the latest standards.

Example

Vijio allows for the tracking of reported adverse events over time, providing analytics and reports that help identify trends or patterns which may require further investigation or action.

Scenario

A healthcare provider observes an increase in a particular type of adverse event. Using Vijio, they can generate a report of all similar events to analyze if there is a potential link to a specific batch of medication or a broader safety concern.