Detect safety signals early. Stay compliant automatically.
Pharmacovigilance automation built for modern life sciences. Screver AI continuously scans feedback, forms, and digital touchpoints for potential adverse events – alerting your PV teams instantly, with full traceability and audit-ready logs.
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Pharma Domain-Trained Intelligence
Understands medical, therapeutic, and regulatory terminology with pharma-trained AI models.
Omnichannel Data Coverage
Monitors safety-related mentions across websites, surveys, portals, CRMs, and call logs in one unified workflow.
Compliant & Traceable Alerts
Every event is logged with full audit history and automated report generation for internal or external safety teams.
Built for omnichannel healthcare environments
Screver monitors unstructured feedback across every touchpoint – from websites, surveys, and call transcripts to CRMs and chatbots.
It continuously listens for spontaneous mentions of side effects or safety concerns, turning raw text into structured, compliant data streams ready for pharmacovigilance review.
From signals to safety actions – powered by custom RAG and your Company & Brand IQ
Every company, therapy area, and product has its own terminology. That’s why Screver RAG-based AI is trained on your Brand IQ – integrating your products list, safety keywords, and internal documentation. The system uses this context to distinguish between relevant and irrelevant mentions, reducing false positives and increasing accuracy over time.
Enriched with your product labels, brand terms, and indication data
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Understands context beyond keywords – differentiating “headache” in AE vs. non-AE contexts
Continuously learns from human validation and updates detection logic
Automated reports and alerts – in real time or daily summaries
Once a potential event is confirmed, Screver automatically notifies the right pharmacovigilance or local safety team. Reports can be triggered instantly or consolidated into daily or weekly safety summaries, with full traceability and audit logs.
· Real-time alerts for critical mentions or specific drugs
· 24h or weekly summaries with all validated AE cases
· Automated PDF or dashboard exports to Power BI, Qlik, or internal systems
AI Agents for Adverse Event Monitoring
Detects side effects or safety mentions in open text unstructured feedback and automatically alerts your Pharmacovigilance team.
Our approach to Adverse Event Monitoring
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Co-Develop & Pilot – Start small, test fast, prove value
We start with people, not processes. Each pilot measures how teams react to new initiatives, leadership styles.
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Refine & Align – Optimize workflows and metrics before scaling
We start with people, not processes. Each pilot measures how teams react to new initiatives, leadership styles.
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Expand confidently and let AI guide progress.
The results shape stronger cultures, better communication, and measurable improvement.
Want to launch or improve your Voice of Customer program?
Share a few details, and our team will get in touch to co-create a plan tailored to your products, markets, and therapeutic area.
Screver IQ Resources
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“A congress isn’t just an event; it’s the start of a relationship. Using Screver, we turned every interaction into a moment to listen, engage, and prepare better for each launch.”
