The Icelandic Medicines Agency is Iceland's national competent authority for medicines. As an EEA country, Iceland participates in the European medicines regulatory and pharmacovigilance framework.
Core official resources
- Icelandic Medicines Agency — national authority and medicine-safety information.
- EMA GVP.
- EudraVigilance.
Practical use
Use IMA for Iceland-specific reporting contacts, national safety communications and local implementation questions while applying the EEA/EU pharmacovigilance framework for harmonised procedures.