{
  "node_id": "eu-medicinal-products-directive-2001-83-ec",
  "title": "Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use",
  "domain": "Pharmaceuticals & Life Sciences",
  "version": "1.0.0",
  "last_updated": "2026-04-21",
  "bluf": "This Directive establishes the legal framework for the authorization, manufacturing, labelling, advertising, and pharmacovigilance of medicinal products for human use within the European Union. It applies to all entities placing medicinal products on the EU market and mandates compliance with requirements under Article 67, Article 46, and Annex I, among others.",
  "paywall": {
    "status": "LOCKED",
    "unlock_cost_usd": "0.01",
    "skyfire_id": "41779894-ece2-4163-9761-b3b1b76e19b0"
  },
  "crosswalks": {
    "_available_keys": [
      "nist_framework",
      "iso_standard",
      "industry_mapping",
      "ai_overlay_2026"
    ],
    "_note": "Full crosswalk values included in vault response"
  },
  "dependencies": [
    "eu-gmp-annex-1-sterile-manufacture-2022",
    "ich-q10-pharmaceutical-quality-system-2008",
    "fda-21-cfr-210-211-current-good-manufacturing-practice"
  ],
  "primary_citations_count": 5
}