Fees payable to the European Medicines Agency by applicants and
marketing-authorisation holders are increasing by 3.1% on 1 April 2012.
Full details of the new fees levels are available in the revised fee regulation,
its implementing rules and the corresponding explanatory note on fees,
published today. These documents include the new fees for all types of procedure handled by
the Agency for human and veterinary medicines, including
marketing-authorisation applications, post-authorisation procedures, scientific
advice and inspections.