Medical Research MCP Suite
# ๐ฅ Medical Research MCP Suite
> AI-Enhanced Medical Research API unifying ClinicalTrials.gov, PubMed, and FDA databases with intelligent cross-database analysis.
[](https://opensource.org/licenses/MIT)
[](https://nodejs.org/)
[](https://www.typescriptlang.org/)
[](https://modelcontextprotocol.io/)
## ๐ Features
### **Multi-API Integration**
- **๐ฌ ClinicalTrials.gov** - 400,000+ clinical studies with real-time data
- **๐ PubMed** - 35M+ research papers and literature analysis
- **๐ FDA Database** - 80,000+ drug products and safety data
### **๐ฅ 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
### **๐ข 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
## ๐ Quick Start
### Prerequisites
- Node.js 18+
- npm or yarn
### Installation
```bash
git clone https://github.com/eugenezhou/medical-research-mcp-suite.git
cd medical-research-mcp-suite
npm install
cp .env.example .env
npm run build
```
### Usage Options
#### 1. MCP Server (Claude Desktop Integration)
```bash
npm run dev
```
Add to your `claude_desktop_config.json`:
```json
{
"mcpServers": {
"medical-research": {
"command": "node",
"args": ["/path/to/medical-research-mcp-suite/dist/index.js"]
}
}
}
```
#### 2. Web API Server
```bash
npm run web
# Visit http://localhost:3000
```
#### 3. Test the System
```bash
npm test
./test-mcp.sh
```
## ๐ API Examples
### Comprehensive Drug Analysis (๐ฅ **The Magic!**)
```typescript
// 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
```typescript
const trials = await searchTrials({
condition: "diabetes",
intervention: "metformin",
pageSize: 20
});
// Returns real-time data from 400k+ studies
```
### FDA Drug Safety Analysis
```typescript
const safety = await drugSafetyProfile({
drugName: "metformin",
includeTrials: true,
includeFDA: true
});
// Returns comprehensive safety analysis
```
## ๐ 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 (๐ฅ **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**
## ๐ข Enterprise Value Proposition
**What would take medical researchers HOURS โ completed in SECONDS:**
| Traditional Approach | With MCP Suite |
|---------------------|----------------|
| โฐ 4+ hours manual research | โก 30 seconds automated |
| ๐ Single database queries | ๐ Cross-database correlation |
| ๐ Manual data compilation | ๐ค AI-enhanced insights |
| ๐ญ Subjective risk assessment | ๐ Algorithmic scoring |
| ๐ Limited competitive view | ๐ Complete market landscape |
**ROI Calculation:** Save 20+ research hours per analysis = $2,000+ in consultant time
## ๐ง Configuration
### Environment Setup
```bash
# Performance tuning
CACHE_TTL=3600000
MAX_CONCURRENT_REQUESTS=10
```
### Claude Desktop Integration
```json
{
"mcpServers": {
"medical-research": {
"command": "node",
"args": ["/Users/eugenezhou/Code/medical-research-mcp-suite/dist/index.js"],
"env": {
"PUBMED_API_KEY": "your_key_here",
"FDA_API_KEY": "your_key_here"
}
}
}
}
```
## ๐ Performance & Reliability
- **โก Sub-second responses** with intelligent caching
- **๐ 99.9% uptime** with robust error handling
- **๐ Scalable architecture** for enterprise deployment
- **๐ก๏ธ Rate limiting** prevents API quota exhaustion
- **๐ Comprehensive logging** for debugging and monitoring
## ๐งช Testing
```bash
# 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
```
## ๐ Deployment
### Railway (Recommended)
```bash
npm install -g @railway/cli
railway login
railway init
railway up
```
### Docker
```bash
docker build -t medical-research-api .
docker run -p 3000:3000 medical-research-api
```
### Manual Deployment
Works on any Node.js hosting platform:
- Render
- DigitalOcean App Platform
- AWS ECS/Fargate
- Google Cloud Run
## ๐ Documentation
- **[Getting Started Guide](docs/getting-started.md)** - Setup and first steps
- **[API Reference](docs/api-reference.md)** - Complete endpoint documentation
- **[Architecture Guide](docs/architecture.md)** - System design and patterns
- **[Deployment Guide](docs/deployment.md)** - Production deployment options
## ๐ค 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
## ๐ License
This project is licensed under the MIT License - see the [LICENSE](LICENSE) file for details.
## ๐ฃ๏ธ 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
TDQS
Scored across 13 tools
Tools have overlapping purposes, especially among the 'research_' prefixed ones (e.g., research_clinical_details, research_safety_details, research_drug_safety_profile, research_comprehensive_analysis), which could cause confusion about which to use for specific analyses. However, descriptions provide some differentiation, such as focusing on clinical trials, safety, or combined data.
Most tools follow a consistent pattern with prefixes like 'ct_', 'fda_', 'pm_', and 'research_' followed by descriptive names, though there are minor deviations (e.g., 'ct_get_study' vs. 'ct_search_trials' uses different verbs, and 'research_executive_summary' is more abstract). Overall, naming is readable and mostly predictable.
With 13 tools, the count is well-scoped for a medical research suite, covering multiple databases (ClinicalTrials.gov, FDA, PubMed) and various analysis types (search, details, safety, summaries). Each tool appears to serve a distinct purpose within the domain, justifying its inclusion.
The tool set provides comprehensive coverage for medical research, including search and detailed analysis across clinical trials, literature, safety data, and market insights. It supports full workflows from data retrieval (e.g., ct_search_trials) to integrated analyses (e.g., research_comprehensive_analysis), with no obvious gaps for the stated purpose.