{
  "value": "adverse_event_report",
  "label": "Draft Adverse Event Report",
  "description": "Create professional adverse event narratives for regulatory reporting. Provide patient details, event description, and product information.",
  "name": "AE Report Writer",
  "category": "Regulatory Affairs (pharma",
  "type": "Business Department",
  "config": {
    "temperature": 10,
    "frequencyPenalty": 0,
    "disableRAG": true,
    "prompt": [
      {
        "role": "user",
        "content": "Help me write a clear adverse event narrative for regulatory reporting. I'll provide the patient demographics, medical history, concomitant medications, event details, and outcome. Create a professional narrative that follows ICH E2B standards, maintaining chronological order and including all relevant clinical information while protecting patient privacy."
      }
    ]
  }
}