In-line & Release Testing

Workflow steps

1. Manufacturing (EU-GMP Site)
   EU Pharmacopoeia is the reference standard for Danish market.
2. GACP + IPC
   Full GACP and in-process controls per EU-GMP.
   • EU GACP or WHO GACP
   • HPLC IPC at manufacturing stages
   • Environmental monitoring
3. Finished Product Testing
   Full release panel per EU Pharmacopoeia and DKMA product specifications.
   • THC/CBD assay (HPLC)
   • Microbiological per Ph. Eur.
   • Pesticide residues (EU MRL)
   • Heavy metals, mycotoxins
   • Moisture content
4. QP Release
   EU QP certifies batch. Danish language not required for batch certificate — English accepted by DKMA.
   • QP named on Danish wholesale authorization
   • Full batch record reviewed
5. Batch Released ✓
   Available for Danish pharmacy distribution.