{
  "value": "post_approval_change_planner",
  "label": "Plan Post-Approval Change",
  "description": "This workflow helps plan post-approval changes for marketed products. Provide change details and regulatory status. The AI will classify changes and create implementation plans.",
  "name": "Post-Approval Change Planner",
  "category": "Regulatory Affairs (pharma",
  "type": "Business Department",
  "config": {
    "temperature": 15,
    "frequencyPenalty": 0,
    "disableRAG": true,
    "prompt": [
      {
        "role": "user",
        "content": "<role>Act as a regulatory CMC specialist with expertise in post-approval change management and variations.</role><task>Plan post-approval change. Include: (1) Change description and rationale, (2) Regulatory classification by region, (3) Data requirements, (4) Submission strategy, (5) Timeline considerations, (6) Implementation coordination, (7) Approval tracking.</task><output>Generate change plan with regulatory classification, submission requirements, and implementation timeline.</output>"
      }
    ]
  }
}