{
  "id": "workflow:drug-approval-pipeline",
  "_kind": "Workflow",
  "_file": "workflows/workflows/workflows-expanded-3.yaml",
  "_cluster": "workflows",
  "attributes": {
    "displayName": "Drug Approval Pipeline",
    "workflowKind": "operational",
    "triggerType": "event-driven",
    "typicalCadence": "per-drug",
    "complexity": "cross-team",
    "description": "Regulatory drug approval process — pre-clinical data compilation,\nIND/NDA/BLA submission preparation, regulatory agency correspondence,\nadvisory committee preparation, and post-approval commitments tracking.\nCoordinates across clinical, regulatory, and manufacturing teams.\n"
  },
  "outgoingEdges": [
    {
      "from": "workflow:drug-approval-pipeline",
      "to": "role:clinical-data-scientist",
      "kind": "involves_role",
      "attributes": {}
    },
    {
      "from": "workflow:drug-approval-pipeline",
      "to": "role:compliance-officer",
      "kind": "involves_role",
      "attributes": {}
    },
    {
      "from": "workflow:drug-approval-pipeline",
      "to": "role:research-scientist",
      "kind": "involves_role",
      "attributes": {}
    },
    {
      "from": "workflow:drug-approval-pipeline",
      "to": "domain:pharmaceuticals",
      "kind": "applies_to_domain",
      "attributes": {}
    },
    {
      "from": "workflow:drug-approval-pipeline",
      "to": "domain:healthcare",
      "kind": "applies_to_domain",
      "attributes": {}
    },
    {
      "from": "workflow:drug-approval-pipeline",
      "to": "responsibility:drug-safety-monitoring",
      "kind": "triggers_responsibility",
      "attributes": {}
    },
    {
      "from": "workflow:drug-approval-pipeline",
      "to": "responsibility:regulatory-reporting",
      "kind": "triggers_responsibility",
      "attributes": {}
    }
  ],
  "incomingEdges": []
}