{
  "value": "clinical_trial_protocol_summary",
  "label": "Summarize Clinical Trial Protocol",
  "description": "Create executive summaries of clinical trial protocols for regulatory submissions. Paste the full protocol or key sections.",
  "name": "Protocol Summary",
  "category": "Regulatory Affairs (pharma",
  "type": "Business Department",
  "config": {
    "temperature": 10,
    "frequencyPenalty": 0,
    "disableRAG": true,
    "prompt": [
      {
        "role": "user",
        "content": "Create an executive summary of this clinical trial protocol. Include the study objectives, design, population, primary and secondary endpoints, sample size, and key inclusion/exclusion criteria. Format it clearly with sections and bullet points. Keep the summary under one page and highlight any novel or critical aspects for regulatory review."
      }
    ]
  }
}