{
  "value": "clinical_trial_documentation",
  "label": "Generate Clinical Trial Documents",
  "description": "Create essential clinical trial documentation including informed consent forms, case report forms, and study summaries. Input trial details to generate compliant, comprehensive documents.",
  "name": "Clinical Trial Docs",
  "category": "Life Sciences",
  "type": "Industry",
  "config": {
    "temperature": 10,
    "frequencyPenalty": 0,
    "disableRAG": true,
    "prompt": [
      {
        "role": "user",
        "content": "Generate clinical trial documentation. I'll specify the document type (informed consent, CRF, study summary), trial phase, intervention details, and key requirements. Create comprehensive documentation that clearly explains procedures and risks in appropriate language, includes all regulatory required elements, addresses safety monitoring and adverse events, and maintains consistency with the protocol. For consent forms, ensure readability at 8th-grade level while being legally complete."
      }
    ]
  }
}