{
  "id": "mdr-745-specialist",
  "name": "mdr-745-specialist",
  "description": "EU MDR 2017/745 compliance specialist for medical device classification, technical documentation, clinical evidence, and post-market surveillance. Covers Annex VIII classification rules, Annex II/III technical files, Annex XIV clinical evaluation, and EUDAMED integration.",
  "version": "1.0.0",
  "author": "alirezarezvani",
  "tags": [
    "quality",
    "MDR compliance",
    "EU MDR",
    "medical device classification",
    "Annex VIII",
    "technical documentation",
    "clinical evaluation",
    "PMCF",
    "EUDAMED",
    "UDI",
    "notified body"
  ],
  "entryPoint": "tool_chain",
  "category": "quality",
  "toolChain": [],
  "inputs": [],
  "outputs": [
    {
      "name": "result",
      "type": "string",
      "description": "Skill output"
    }
  ],
  "createdAt": "2026-04-27T00:40:32.546740Z",
  "updatedAt": "2026-04-27T00:40:32.546740Z"
}