{
  "value": "clinical_trial_documentation",
  "label": "Generate Clinical Trial Documentation",
  "description": "Create required documentation for clinical trials. Provide trial protocol details, patient data, and regulatory requirements to generate compliant trial documents.",
  "name": "Trial Documentation",
  "category": "Clinical Operations (healthcare)",
  "type": "Business Department",
  "config": {
    "temperature": 10,
    "frequencyPenalty": 0,
    "disableRAG": true,
    "prompt": [
      {
        "role": "user",
        "content": "Create clinical trial documentation. I'll provide the trial protocol, inclusion/exclusion criteria, and specific documentation needs. Generate the required documents such as informed consent forms, case report form templates, or standard operating procedures. Ensure compliance with Good Clinical Practice guidelines and make the language appropriate for the intended audience."
      }
    ]
  }
}