Monitor scientific publications and identify safety signals with traceable evidence.
Automate literature scanning, extract adverse event mentions, and link findings to drugs, reactions, and sources. Support ongoing signal detection and periodic safety reporting with verifiable audit trails.
Faster Signal Detection
Entity Extraction Accuracy
Audit Trail Coverage
Sources Supported
Literature Monitoring & Signal Detection unifies data from scientific journals, clinical studies, and medical databases to support pharmacovigilance operations. It automatically screens publications for drug-event co-mentions, normalizes entities to MedDRA or WHO-DD standards, and highlights potential safety signals for review. Each signal is traceable to its originating publication, abstract, or paragraph, ensuring audit compliance. Configurable workflows allow safety and medical reviewers to confirm, annotate, or close signals. Periodic outputs feed into aggregate reporting, enabling continuous, documented oversight of product safety trends.
Explore how literature sources are ingested, analyzed, and cross-referenced — turning unstructured publications into structured, traceable pharmacovigilance insights.
Set up AI capabilities quickly using intuitive, low-code tools.
Deploy AI systems seamlessly and scale them efficiently.
Track performance metrics and continuously refine operations.
Integrate feedback loops to adapt and improve your solutions.
