Our solution automates and accelerates case intake by extracting and categorizing adverse events and product inquiries from various sources in real time, improving efficiency and accuracy.

Our solution uses AI to extract adverse events, product complaints and medical inquiries from online sources, automatically categorizing them with precision using the MedDRA and WHO drug dictionary. This streamlines both reporting and analytics processes.

Our system employs GenAI to assist in creating aggregate reports and RMP, automating content generation (assisted authoring) while ensuring compliance with industry standards and guidelines.

Our solution ensures data integrity and compliance by implementing automated data entry checks during case processing. This helps reduce errors and enhances the overall quality of ICSR (individual case safety reports).

Our data analytics dashboard empowers users to transform data into actionable insights. With real-time interactive reports and customizable features, users can explore, analyze, collaborate and scale across the organization. The dashboard also includes built-in governance and security measures.