Automated Literature Search & Extraction
- • Scans journals, regulatory docs, and registries using AI & NLP
- • Efficiently extracts key safety data and adverse events
- • Minimizes manual effort for your team
Signal Detection & Risk Assessment
- • AI highlights critical adverse events in extracted content
- • Flags and ranks signals by impact & seriousness
- • Empowers early response to safety risks
Automated Review & Real-Time Reporting
- • Auto-reviews safety trends in the literature
- • Instantly generates shareable compliance reports
- • Consistent, auditable documentation
Integration & Cross-System Sync
- • Connects seamlessly with Argus, Veeva Vault, and more
- • Keeps safety databases updated with literature findings
- • Ensures prompt action and workflow harmony
Regulatory Compliance & Audit Readiness
- • Built for FDA, EMA, ICH, and global standards
- • Maintains audit-ready logs for 21 CFR Part 11
- • Ensures secure, confidential data handling
Real-Time Alerts & Notifications
- • Custom alerts for key risks and new safety content
- • Notifies teams and stakeholders instantly
- • Enables rapid, proactive responses
Why Choose SafeVig Digital Literature?
- Efficiency Through Automation: AI automates search, extraction, and review—saving time and resources.
- Intelligent Signal Detection: Detects even subtle safety trends with AI & NLP.
- Seamless Integration: Works effortlessly with your pharmacovigilance systems.
- Global Compliance: Aligned with FDA, EMA, ICH, and audit-ready by design.
- Real-Time Alerts: Stay ahead of safety risks with instant notifications.
- Data Security: Robust encryption and access control ensure confidentiality.
Empowering Pharmacovigilance with SafeVig Digital Literature
Modernize your literature monitoring with SafeVig's AI-powered automation.
Detect signals earlier, respond faster, and ensure full regulatory compliance.
