Our solution automates and accelerates case intake by extracting and categorizing adverse events, product quality issues and medical inquiries from diverse sources, ensuring real-time data capture and categorization

Our AlertAE solution can ingest, identify and extract adverse events, product quality complaints and medical inquiries from multiple digital media channels. It employs AI-driven classification to auto-populate fields and accurately code medical terms with MedDRA and medicinal products with the WHO drug dictionary. This streamlines reporting, analytics and signaling processes

Employs Gen AI to assist in the creation of aggregate reports and RMP, automating content generation (assisted authoring) and ensuring compliance with industry standards and guidelines

Ensures data integrity and compliance by implementing automated data entry checks during case processing to help reduce errors and enhance the overall quality of ICSR (individual case safety report)

Empowers users to transform data into actionable visuals —and with built-in governance and security measures plus real-time interactive reports and customizable features, users can explore, analyze, collaborate and scale across the organization

Identify potential case quality issues early, rectify errors and increase regulatory submissions' quality

Best-in-class medical inquiry management for informed decisions

A 360 suite of client-based services in the GPV&E space, including clinical development, post-marketing and regulatory requirements

Tackle the complexity of diverse data sources, automate critical processes and streamline workflow management by leveraging advanced AI technology

Intelligent identification and classification of adverse events, product quality complaints and medical inquiries