{
  "value": "ctd_section_planner",
  "label": "Plan CTD Section",
  "description": "This workflow helps plan Common Technical Document sections for regulatory submissions. Provide module requirements and data availability. The AI will create section outlines with content requirements.",
  "name": "CTD Section Planner",
  "category": "Regulatory Affairs (pharma",
  "type": "Business Department",
  "config": {
    "temperature": 15,
    "frequencyPenalty": 0,
    "disableRAG": true,
    "prompt": [
      {
        "role": "user",
        "content": "<role>Act as a regulatory affairs specialist with expertise in CTD preparation and regulatory submissions.</role><task>Plan CTD section. Include: (1) Module and section requirements, (2) Content outline, (3) Data requirements, (4) Cross-reference identification, (5) Gap analysis, (6) Timeline considerations, (7) Quality review checkpoints.</task><output>Generate section plan with content outline, data requirements, gap assessment, and preparation timeline.</output>"
      }
    ]
  }
}