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Import Authorization

CCBM authorization and OMC process for medicinal cannabis imports

Import / Export Verified 2026-04-20

Workflow steps

  1. Import Intent
    You intend to import medicinal cannabis into the Netherlands. The Netherlands has a unique dual system: OMC (Office of Medicinal Cannabis) handles government-tendered supply; private imports occur via CCBM authorization.
    • CCBM import authorization (per shipment)
    • IGJ-licensed importer / wholesale dealer
    • EU-GMP Part I certificate mandatory for finished product
  2. OMC tender or private import?
    OMC manages the government tender for standardised cannabis products supplied to Dutch pharmacies. Private imports are for non-tendered products via CCBM authorization.
  3. OMC Tender Pathway — Government supply channel
    OMC issues tenders for standardised cannabis products (Bedrocan varieties). Only OMC-contracted suppliers may supply these products to Dutch pharmacies.
    • Respond to OMC public tender
    • EU-GMP Part I certification required
    • Product must meet OMC standardisation requirements
    • OMC contracts awarded for 2–4 year periods
  4. Private Import — CCBM — Non-tendered products
    Bureau for Medicinal Cannabis (CCBM) authorizes per-shipment imports of non-OMC products. Required for branded products, novel formulations, or foreign-manufactured cannabis not in OMC tender.
    • CCBM import authorization per shipment
    • Dutch licensed importer as sponsor
    • EU-GMP Part I for finished product mandatory
  5. Apply: CCBM Import Authorization
    Application to Bureau for Medicinal Cannabis. Submit product documentation, GMP/GACP certificates, and exporting country authorization.
    • Product specifications and COA
    • EU-GMP Part I certificate
    • GACP certificate
    • Exporting country export authorization
    • Processing: approximately 3–5 weeks
  6. Authorization granted?
    CCBM issues or requests additional information. Common issues: GMP certificate scope, product labeling in Dutch, or GACP certificate currency.
  7. Address CCBM Queries
    Respond to CCBM in writing. Dutch-language labeling is commonly flagged — ensure labeling complies with Dutch Medicines Act.
    • Dutch-language product labeling
    • Updated certificates if flagged
  8. Authorization Issued
    Per-shipment CCBM authorization issued. Valid for the specific product, quantity, and supplier.
    • Original must accompany shipment
    • Rotterdam port or Amsterdam Schiphol — primary entry points
  9. Dutch Customs Entry
    Customs clearance at Rotterdam (sea) or Schiphol (air). Opium Act declaration required. CCBM authorization presented.
    • CCBM authorization (original)
    • Opium Act import declaration
    • All shipping documents + COA
  10. Shipment Cleared ✓
    Released to licensed Dutch importer/distributor. QP certification required before pharmacy supply.
Regulatory Hierarchy