An invoice will be issued to the applicant after IMA has received an application.
IMA collects fees according to the following tariffs:
- TARIFF for marketing authorisations, annual fees and other licence fees for medicinal products and other related products, collected by the Icelandic Medicines Agency.
- In the event of any discrepancy between the Icelandic and English versions of the tariff, the Icelandic version shall prevail.
In cases where independent external experts are required to assess the data, a separate charge will be added for their work in addition to the standard fee. Such charges are authorized as per Articles 1 and 2 of the Tariff for Marketing Authorisation Fees, Annual Fees and Other Fees for Medicinal Products Collected by the Icelandic Medicines Agency, published in April 2026. Refer also to Articles 7 and 89 of the Medicines Act. Should such additional costs arise, the applicant will be notified in advance.