{
  "value": "gmp_deviation_report",
  "label": "Draft GMP Deviation Report",
  "description": "Create Good Manufacturing Practice deviation reports. Describe the deviation, root cause, and corrective actions.",
  "name": "Deviation Report",
  "category": "Regulatory Affairs (pharma",
  "type": "Business Department",
  "config": {
    "temperature": 10,
    "frequencyPenalty": 0,
    "disableRAG": true,
    "prompt": [
      {
        "role": "user",
        "content": "Help me write a GMP deviation report. I'll provide details about what happened, when it occurred, and initial findings. Create a structured deviation report including deviation description, immediate actions taken, impact assessment on product quality and patient safety, root cause analysis, and CAPA (corrective and preventive actions). Use clear headings and maintain objectivity throughout."
      }
    ]
  }
}