AI Integration

Connect AI Assistants — and Verify Every Answer

Give Claude and other AI assistants live access to your ClinicaLister portfolio through the Model Context Protocol (MCP) — the verifiable access layer. Ask in natural language, run cross-portfolio analysis, and drill into the provenance-backed source record behind any answer. No manual exports.

74
Live Data Tools
58
AI Report Recipes
3
Enrichment Resources

Why AI Integration?

The Problem

Extracting insights requires manual exports, formatting for analysis tools, re-running queries when data changes. AI assistants can help — but without direct access, every interaction starts with copy-pasting.

The Solution

MCP integration connects your AI assistant directly to your trial portfolio, drug intelligence, device data, monitoring alerts, and saved queries. Ask questions in natural language, get answers grounded in live regulatory data.

What Is MCP?

The Model Context Protocol is an open standard that allows AI assistants to securely access external data sources.

Your AI assistant understands your trial portfolio the same way you do — referencing specific trials, comparing drug timelines, surfacing alerts, and cross-referencing safety data with direct access to your live data.

Setup in Under Two Minutes

Industry-standard OAuth2 authentication secures the connection.

1

Navigate to Settings → MCP Integration tab

2

Click "Generate Credentials" for Client ID and Secret

3

In claude.ai, go to Customize → Connectors → "+"

4

Enter your ClinicaLister Server URL and credentials

5

Click Connect — live access to your trial portfolio

What Your AI Assistant Can Access

Trial Portfolio

Followed trials with metadata, custom columns, contacts, locations

Drug Intelligence

29,600+ FDA drugs, 2,700+ EMA medicines, patents, FAERS, pricing

Device Intelligence

177,000+ device submissions, GUDID, MAUDE reports, recalls

Monitoring & Changes

Trial modifications with severity, change history, audit trails

Saved Queries

Execute saved queries, access filter criteria

Use Cases

Portfolio Briefing

"Summarize all Phase III oncology trials in my portfolio that changed status in the last 30 days."

Competitive Intelligence

"Which sponsors have the most trials targeting PD-L1? Are any linked drugs approaching patent expiration?"

Regulatory Risk

"List all trials linked to drugs with active FDA boxed warnings or REMS requirements."

Safety Signal Review

"Show device adverse events reported last quarter for devices linked to my orthopedic trials."

Export Preparation

"Create a summary of top 10 drugs by trial count, including exclusivity end dates and biosimilar competition."

Two Ways to Work with AI

Live MCP Connection

Live queries against current data. Best for interactive analysis, ad-hoc questions, ongoing monitoring.

Agent-Ready Export

Structured XLSX with 22 data sheets + embedded AI prompt. Best for deep offline analysis.

Use both together: live connection for day-to-day, structured export for comprehensive reviews.

Security

OAuth2 AuthenticationIndustry-standard credential flow

Encrypted at RestAES-256 encryption for client secrets

Account-Scoped AccessRow-Level Security isolation

Instant RevocationRevoke credentials anytime

No Data Stored by AIData provided on demand, not cached

Why the answers are grounded

The AI isn't guessing across raw tables — it reads our knowledge graph.

Because every drug, disease, and device resolves to a canonical identity with typed, confidence-scored links, an assistant can answer “every trial for this molecule and its biosimilars, with the regulatory and pricing context” in a single hop — and attach provenance to every claim. The knowledge graph is what turns live data access into trustworthy answers.

Ready to give your AI assistant access to verifiable regulatory intelligence?