Turning Literature into Actionable Safety Insights
Literature monitoring ensures that relevant safety information from published sources is continuously identified and assessed. SCIOM provides structured monitoring across global and local literature, including journals, conference proceedings, and regional publications, to capture potential adverse events and emerging safety signals.
All relevant findings are evaluated and integrated into the pharmacovigilance system to support early signal detection, regulatory compliance, and ongoing benefit–risk assessment.
Talk to Our PV ExpertsDesigned for Accuracy. Built for Continuous Monitoring.
Comprehensive Global & Local Coverage
Monitoring across journals, conference proceedings, and regional publications to ensure no relevant data
is missed
AI-Driven Literature Screening
Faster identification of relevant articles through automated filtering, duplicate detection, and
prioritization
Structured Classification of Safety Data
Articles categorized into ICSR, signal, and aggregate-related information for streamlined processing
Early Safety Signal Identification
Detection of emerging risks from published data to support proactive pharmacovigilance
Seamless PV System Integration
Literature findings integrated directly into the safety database for unified signal analysis
Support for Aggregate Reporting
Literature insights aligned with PSUR, PBRER, and DSUR requirements
Customized Search Strategies
Tailored monitoring based on product, indication, and therapeutic area
Automated Tracking & Reporting
Continuous tracking, trending, and reporting of literature-derived safety information
Where Literature Becomes Safety Insight
Our literature monitoring capabilities are designed to ensure comprehensive identification, evaluation, and integration of safety information from published sources.
Consistent Monitoring. Reliable Outcomes.
Faster - AI-driven literature screening for timely ICSR and signal detection
Global Coverage – Continuous monitoring of scientific publications worldwide
Integrated – Literature cases mapped to the main safety database with XML conversion
Compliance-ready outputs with full traceability
Clarity at Every Step of Monitoring
AI-driven search across global and local literature databases, journals, conference proceedings, and other publications.
Duplicate removal, relevance filtering, and categorization of articles into ICSR, signal, or aggregate-related information.
Valid ICSRs extracted and submitted into the safety database, ensuring full traceability and regulatory compliance.
Potential safety signals highlighted for review by PV specialists and medical reviewers.
Literature findings integrated with aggregate reports, signal detection dashboards, and safety committee updates for proactive risk management.
Comprehensive Coverage. Reliable Safety Insights.
Qualified medical and scientific reviewers with strong pharmacovigilance expertise
AI-enabled literature surveillance for faster and more accurate identification of safety signals
Seamless integration with pharmacovigilance systems and safety databases for unified data management
Automated global coverage to ensure early detection of emerging patient safety information
Quality oversight with regulatory-ready documentation aligned with global pharmacovigilance requirements
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