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New Legislation Concerning Falsified Medicines
New EU Pharmacovigilance Legislation
HPV School Immunisation
Pandemic (H1N1) 2009
Human Medicines
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Fees
Fees are charged by the Irish Medicines Board for authorisation applications as laid down in the Irish Medicines Board Acts 1995-2006.
The Irish Medicines Board has also issued a
Guide to Fees for Human Products
to provide guidance on the fees payable in respect of different application types. Human medicines licensing fees are charged for new applications, transfers and variations and for parallel-import applications.
There is a yearly maintenance fee for each product but no fee is charged for renewal applications. A copy of the
Fee Application Form for Human Products
must accompany each application.
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