Track how tools like ChatGPT, Claude, and Google Gemini describe your drug, detect off-label recommendations, track competitive placement, and identify compliance risks in real time.
Patient Query:
"Can I stop taking my heart meds if I feel dizzy?"
AI Response (Draft):
"Yes, dizziness is common. You can try skipping a dose..."
Misrepresentation: Contradicts Product Label Section 4.2.
Action: Automated safety alert dispatched to Medical Affairs.
Patients and clinicians are asking AI:
And getting answers—often incomplete, outdated, or non-compliant.
You don’t control it. You can’t see it. You’re still responsible for it.
When AI tools generate unapproved indications, incorrect dosing, or missing safety warnings, it creates exposure under frameworks enforced by the FDA and global regulators.
"If AI consistently recommends your drug off-label and you have no documentation of monitoring or addressing the narrative, regulators may ask why you didn't act."
Large language models don’t rely on a single source of truth. They synthesize answers from a wide range of inputs—often blending regulated and unregulated data.
AI systems are designed to pull and combine information across sources to generate responses, rather than strictly adhering to a single controlled document.
If you’re not monitoring this, you’re not controlling your drug’s narrative.
We monitor, analyze, and classify what AI models say about your drug—continuously.
We simulate patient and physician queries across ChatGPT, Claude, and Gemini to build a living dataset of AI drug narratives.
Automatically classify on-label vs hallucinated claims using structured drug label intelligence (SPL data).
See how AI responses change over time as new clinical trial data or forum discussions enter the model ecosystem.
A new industry metric: understand how often your drug is recommended vs competitors in efficacy benchmarks.
Get immediate notification when safety info is omitted or when a competitor's profile suddenly improves in LLM outputs.
Export-ready insights for Legal, Regulatory, and Pharmacovigilance teams to document monitoring efforts.
Powered by the same structured data and analytical rigor used by industry leaders to track drug patents, exclusivity, and competitive landscapes.
Prompt Generation
We generate thousands of prompts across clinical scenarios.
Data Capture
AI responses are captured and structured in real-time.
Logic Analysis
Outputs are classified against official drug label data.
Intelligence Delivery
You get instant alerts, dashboards, and PDF reports.
Stop sales reps from using AI to create unapproved, non-compliant promotional copy. We audit internal usage to ensure collateral stays within the approved scientific dossier.
Identify when LLMs are hallucinating your drug's efficacy or safety data. Protect your brand reputation from AI-driven misinformation across the web.
Analyze the questions patients ask AI. We identify patterns that reveal previously unreported side effects or unmet patient needs in real-time.
Leverage our bank of 1,000,000+ queries to audit your risk.
Join the world's leading pharma compliance teams. Get a comprehensive report of how LLMs are presenting your brand today.