| name | clinical-trials |
| description | Design, conduct, and analysis of clinical trials for drug development |
| license | MIT |
| compatibility | opencode |
| metadata | {"audience":"researchers","category":"medicine"} |
What I do
- Design clinical trial protocols
- Understand trial phases (I-IV)
- Analyze trial data and results
- Ensure regulatory compliance
When to use me
When working on clinical trial design or analysis.
Key Concepts
- Trial phases (I, II, III, IV)
- Randomization and blinding
- Sample size calculation
- Endpoints (primary, secondary)
- Informed consent
- FDA/EMA regulations
- Statistical analysis plans