{
  "value": "clinical_monitoring_report",
  "label": "Write Monitoring Visit Report",
  "description": "Write clinical monitoring visit reports for study sites. Provide visit findings to receive structured monitoring reports with observations, action items, and follow-up requirements per GCP standards.",
  "name": "Monitoring Report Writer",
  "category": "Life Sciences",
  "type": "Industry",
  "config": {
    "temperature": 10,
    "frequencyPenalty": 0,
    "disableRAG": true,
    "prompt": [
      {
        "role": "user",
        "content": "<role>Act as a clinical research associate with expertise in GCP monitoring and site management.</role> <task>Write a monitoring visit report based on the findings I describe. Include: (1) visit logistics and attendees, (2) enrollment and retention status, (3) source document verification findings, (4) protocol deviation review, (5) informed consent verification, (6) drug accountability, (7) regulatory document status, (8) safety reporting compliance, (9) action items with responsible parties and deadlines, and (10) overall site performance assessment.</task> <format>Write as a formal monitoring visit report per sponsor requirements.</format>"
      }
    ]
  }
}