Health Products Regulatory Authority. (2022) Guide to import and export licences and letters of no objection for controlled drugs (including the import of cannabis products for medical use). Dublin: Health Products Regulatory Authority.
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External website: https://www.lenus.ie/handle/10147/635103
Operators (manufacturers, wholesalers, authorised persons) require a controlled drugs licence or registration processed by the Health Products Regulatory Authority (HPRA) on behalf of the Department of Health if they wish to produce/manufacture, supply, import, export or possess any controlled drug in the Schedules to the Misuse of Drugs Regulations 2017
B Substances > Cannabis product / compounds (Plant-derived cannabinoids) > Cannabinol / Cannabidiol (CBD oil)
E Concepts in biomedical areas > Medical substance > Prescription drug (medicine / medication)
E Concepts in biomedical areas > Medical substance > Medical / medicinal cannabis
MM-MO Crime and law > Substance use laws > Drug laws
VA Geographic area > Europe > Ireland
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