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In-line & Release Testing

Medicines Authority QC requirements

Testing & QC Verified 2026-04-20

Workflow steps

  1. Manufacturing (EU-GMP Site)
    EU Pharmacopoeia reference standard. Same as all other EU member states.
  2. GACP + Finished Product Testing
    Standard EU-GMP release panel.
    • THC/CBD assay (HPLC)
    • Microbiological per Ph. Eur.
    • Pesticide residues (EU MRL)
    • Heavy metals, mycotoxins
    • Moisture content
  3. QP Batch Release
    EU QP certifies batch for Maltese market release.
    • QP named on Maltese wholesale authorization
    • Full batch record reviewed
  4. Batch Released ✓
    Available for Maltese pharmacy distribution.
Export / Import Process