The import of controlled substances is subject to an import license issued by the Icelandic Medicines Agency, pursuant to Chapter III of Regulation No. 233/2001 on narcotics and other controlled substances, as subsequently amended. The Icelandic Medicines Agency issues import licenses that are valid for the calendar year, except for ephedrine and pseudoephedrine, for which a license must be applied for each time the substance is imported. A license is applied for once a year, and all licenses expire at the end of the year, regardless of when they were applied for.
At the turn of each year, importers must submit information to the Icelandic Medicines Agency on the quantities imported during the preceding year. Furthermore, the importer must provide the Agency with information on the sale of controlled substances if the Agency so requests.
Who can apply?
Importers of controlled substances.
Delivery
Import permits for controlled substances are generally processed within a week from the date the application is received, and the permit is sent by mail to the applicant.
Cost
The cost is according to the fee schedule of the Icelandic Medicines Agency.
Service provider
Icelandic Medicines Agency