Labsco
ezhou89 logo

Medical Research MCP Suite

β˜… 11

from ezhou89

An AI-powered API for medical research, unifying ClinicalTrials.gov, PubMed, and FDA databases with intelligent analysis.

πŸ”₯πŸ”₯πŸ”₯πŸ”₯βœ“ VerifiedAccount requiredNeeds API keys

πŸ₯ Medical Research MCP Suite

AI-Enhanced Medical Research API unifying ClinicalTrials.gov, PubMed, and FDA databases with intelligent cross-database analysis.

License: MIT Node.js Version TypeScript MCP Compatible

🌟 Features

Multi-API Integration

  • πŸ”¬ ClinicalTrials.gov - 400,000+ clinical studies with real-time data
  • πŸ“š PubMed - 35M+ research papers and literature analysis
  • πŸ’Š FDA Database - 80,000+ drug products and safety data

πŸ”₯ AI-Enhanced Capabilities

  • Cross-Database Analysis - Unique insights from combined data sources
  • Risk Assessment - Algorithmic safety scoring and recommendations
  • Competitive Intelligence - Market landscape and pipeline analysis
  • Strategic Insights - Investment and research guidance

🏒 Enterprise Architecture

  • Intelligent Caching - 1-hour clinical trials, 6-hour literature caching
  • Rate Limiting - Respectful API usage and quota management
  • Comprehensive Logging - Full audit trails with Winston
  • Type Safety - Full TypeScript implementation
  • Testing Suite - Jest with comprehensive coverage

πŸ“Š API Examples

Comprehensive Drug Analysis (πŸ”₯ The Magic!)

// Cross-database analysis combining trials + literature + FDA data
const analysis = await comprehensiveAnalysis({
  drugName: "pembrolizumab",
  condition: "lung cancer", 
  analysisDepth: "comprehensive"
});

// Returns:
// - Risk assessment scoring
// - Market opportunity analysis  
// - Competitive landscape
// - Strategic recommendations

Clinical Trials Search

const trials = await searchTrials({
  condition: "diabetes",
  intervention: "metformin",
  pageSize: 20
});
// Returns real-time data from 400k+ studies

FDA Drug Safety Analysis

const safety = await drugSafetyProfile({
  drugName: "metformin",
  includeTrials: true,
  includeFDA: true
});
// Returns comprehensive safety analysis

πŸ›  Available Tools

Single API Tools

  • ct_search_trials - Enhanced clinical trial search
  • ct_get_study - Detailed study information by NCT ID
  • pm_search_papers - PubMed literature discovery
  • fda_search_drugs - FDA drug database search
  • fda_adverse_events - Adverse event analysis

Cross-API Intelligence Tools (πŸ”₯ Unique Value)

  • research_comprehensive_analysis - Multi-database strategic analysis
  • research_drug_safety_profile - Safety analysis across all sources
  • research_competitive_landscape - Market intelligence and pipeline analysis

🏒 Enterprise Value Proposition

What would take medical researchers HOURS β†’ completed in SECONDS:

Traditional ApproachWith MCP Suite
⏰ 4+ hours manual research⚑ 30 seconds automated
πŸ“Š Single database queriesπŸ”„ Cross-database correlation
πŸ“ Manual data compilationπŸ€– AI-enhanced insights
πŸ’­ Subjective risk assessmentπŸ“ˆ Algorithmic scoring
πŸ” Limited competitive view🌐 Complete market landscape

ROI Calculation: Save 20+ research hours per analysis = $2,000+ in consultant time

πŸ“ˆ Performance & Reliability

  • ⚑ Sub-second responses with intelligent caching
  • πŸ”„ 99.9% uptime with robust error handling
  • πŸ“Š Scalable architecture for enterprise deployment
  • πŸ›‘οΈ Rate limiting prevents API quota exhaustion
  • πŸ” Comprehensive logging for debugging and monitoring

πŸ§ͺ Testing

# Run full test suite
npm test

# Test individual components
npm run test:clinical-trials
npm run test:pubmed  
npm run test:fda

# Integration testing
npm run test:integration

# Quick MCP test
./test-mcp.sh

πŸ“š Documentation

🀝 Contributing

  1. Fork the repository
  2. Create your feature branch (git checkout -b feature/amazing-feature)
  3. Commit your changes (git commit -m 'Add amazing feature')
  4. Push to the branch (git push origin feature/amazing-feature)
  5. Open a Pull Request

πŸ“„ License

This project is licensed under the MIT License - see the LICENSE file for details.

πŸ›£οΈ Roadmap

Near Term (1-3 months)

  • WHO International Clinical Trials Registry integration
  • European Medicines Agency (EMA) database support
  • Advanced NLP for literature analysis
  • Real-time safety signal detection

Medium Term (3-6 months)

  • Machine learning models for trial success prediction
  • Integration with electronic health records
  • Patient recruitment optimization tools
  • Regulatory timeline prediction

Long Term (6+ months)

  • Global regulatory database integration
  • AI-powered drug discovery insights
  • Personalized medicine recommendations
  • Integration with pharmaceutical R&D workflows