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C — licensed-product and prescription gated. The Ο περί Ναρκωτικών Φαρμάκων και Ψυχοτρόπων Ουσιών Νόμος (Narcotic Drugs and Psychotropic Substances Law, 29/1977) as amended by Ν. 10(Ι)/2019, with the Κ.Δ.Π. 73/2019 regulations, allows up to three licensed producers to grow, produce and import 'φαρμακευτική κάνναβη' (medical cannabis) for supply to pharmacies, and lets a patient lawfully possess cannabis obtained from a pharmacy on a doctor's prescription.
Κ.Δ.Π. 73/2019 'Οι περί Ναρκωτικών Φαρμάκων και Ψυχοτρόπων Ουσιών (Φαρμακευτική Κάνναβη) Κανονισμοί του 2019' (published 6 March 2019): Reg. 2(1) defines φαρμακευτική κάνναβη as cannabis cultivated, produced, imported, exported, prescribed and supplied to patients 'για την αντιμετώπιση ιατρικών παθήσεων'; Reg. 6(4) caps producer licences at three within a 15-year exclusivity period; Reg. 6(3) selects licensees by 'Πρόσκληση για εκδήλωση ενδιαφέροντος' (call for expressions of interest, €5,000 fee) through a selection committee; the Υπουργός Υγείας (Minister of Health) grants licences (Reg. 21); Reg. 6(2) lets the competent authority import while local production is pending; Reg. 5(5) requires GMP-equivalent certification for imported dry cannabis. Ν. 10(Ι)/2019 amended arts. 7, 7A, 8, 11, 24 and added art. 28A of the basic law to enable licensing regulations, inspectors and administrative fines up to €25,000. No later amendment of the cannabis regulations appears in the 2020–2026 Κ.Δ.Π. indexes.