Regulatory Affairs Department

The Regulatory Affairs Department is part of Icepharma’s Pharmaceutical Division, staffed by experienced specialists in drug registrations and translations. The department provides professional services tailored to client needs, including managing applications and maintenance of marketing authorizations, translating texts, conducting pharmacovigilance and peer reviews, reviewing promotional materials, and liaising with regulatory authorities.

Strict requirements are placed on pharmaceutical distributors in Iceland, with compliance to rigorous laws and regulations. The Regulatory Affairs Department plays a key role in ensuring these standards are met.

The Head of Regulatory Affairs at Icepharma is Elísabet Tómasdóttir.