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Fimea supervises, safeguards and develops

Finnish Medicines Agency

Medicine search Shortages

Etusivun kortti 3

Twitter portlet

Kansalaisille otsikko

For public

Ammattilaisille otsikko

For professionals

Ammattilaisille kortti 1

Pharmacist helping a customer

Special permits

Fimea may grant a special permit for a medicinal product that has no marketing authorisation in Finland to be released for consumption in individual cases for special therapeutic reasons.

Ammattilaisille kortti 2

A doctor inspecting liquid medicine

Assessment of pharmacotherapies (HTA)

Fimea produces and compiles assessments of the therapeutic and economic value of medicines and coordinates the related collaboration. The operations focus on the assessment of new hospital-only medicinal products.

Ammattilaisille kortti 3

Inspector inside a medicine factory

Mandatory reserve supplies

The purpose of legislation concerning mandatory reserve medical supplies is to ensure the availability of medicines in circumstances in which such availability is restricted or prevented as a result of suspension of deliveries, a serious crisis or other equivalent reason.

Ammattilaisille kortti 4

A child

Reporting adverse reactions

An adverse reaction report may be submitted electronically or using the Fimea form.

Ammattilaisille kortti 5

Experts discussing in an EU function

Electronic marketing authorisation submissions

Fimea requests that any submissions related to marketing authorisation applications be conducted electronically whenever possible. Electronic submissions covers almost all applications related to human and veterinary medicines and herbal remedies.

Ammattilaisille kortti 6

Inspector in a medical factory

European Pharmacopoeia

The European Pharmacopoeia is published by the European Directorate for the Quality of Medicines & HealthCare (EDQM) of the Council of Europe in Strasbourg. The publication contains standardised specifications defining the quality of pharmaceutical preparations, their constituents and containers.