{
  "value": "regulatory_submission_checklist",
  "label": "Generate Regulatory Submission Checklists",
  "description": "This workflow creates comprehensive checklists for regulatory submissions. Specify the submission type (IND, NDA, ANDA, etc.), region (FDA, EMA, etc.), and drug/device details, and the AI will generate a detailed checklist of required documents, data, and formatting requirements.",
  "name": "Submission Checklist",
  "category": "Pharmaceuticals",
  "type": "Industry",
  "config": {
    "temperature": 5,
    "frequencyPenalty": 0,
    "disableRAG": true,
    "prompt": [
      {
        "role": "user",
        "content": "Create a detailed regulatory submission checklist based on the submission type and region specified. Organize by major sections (administrative, quality/CMC, non-clinical, clinical, labeling). Include specific document requirements, data needs, and formatting specifications. Add timeline considerations and common pitfalls to avoid. Use checkboxes format for easy tracking. Include references to relevant guidance documents where applicable. Note any region-specific requirements or recent regulatory updates that might apply."
      }
    ]
  }
}