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Import Authorization

DKMA import license process for medicinal cannabis

Import / Export Verified 2026-04-20

Workflow steps

  1. Import Intent
    Denmark has operated a medical cannabis pilot programme since 2018, made permanent in 2021. DKMA (Danish Medicines Agency / Lægemiddelstyrelsen) manages import authorizations. EU-GMP Part I required.
    • DKMA import license per shipment
    • Danish licensed importer
    • EU-GMP Part I mandatory
  2. DKMA Approved Product List
    DKMA maintains a list of approved cannabis products. Suppliers must have their product approved before import authorization is granted.
    • Product must be on DKMA approved list, OR
    • Named patient authorization for unlisted products
    • EU-GMP and GACP certificates submitted with application
  3. Apply: DKMA Import License
    Per-shipment import license from DKMA. Processing: approximately 3–4 weeks.
    • DKMA product approval reference
    • EU-GMP Part I certificate
    • GACP certificate
    • COA per batch
    • Exporting country export authorization
  4. License granted?
    DKMA reviews and issues or requests clarification.
  5. Shipment & Customs
    Copenhagen Airport (CPH) is primary entry point. EU customs procedures apply.
    • DKMA import license (original)
    • All shipping documentation
    • EU customs declaration
  6. Cleared for Danish Market ✓
    Released to licensed Danish importer. QP certifies for Danish market release.
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