{
  "value": "regulatory_submission_checklist",
  "label": "Create Regulatory Submission Checklist",
  "description": "Generate a comprehensive checklist for regulatory submissions. Provide the type of submission (NDA, IND, 510k, etc.) and therapeutic area.",
  "name": "Submission Checklist",
  "category": "Regulatory Affairs (pharma",
  "type": "Business Department",
  "config": {
    "temperature": 10,
    "frequencyPenalty": 0,
    "disableRAG": true,
    "prompt": [
      {
        "role": "user",
        "content": "Create a detailed regulatory submission checklist for me. I'll provide the submission type (like FDA NDA, IND, 510k, or EMA MAA) and the product category. Generate a comprehensive checklist with all required documents, timelines, and key considerations. Organize it by sections and include any pre-submission meeting requirements."
      }
    ]
  }
}