Fees for processing applications
The tables below summarise the fees for clinical trials under the Directive and the Regulation. Fimea charges fees for applications under the Regulation on clinical trials.
More information about Fimea's fees.
Fees for clinical trials under the EU Clinical Trials Directive (2001/20/EC)
New clinical trial 3000 €
Amendments to a clinical trial 1000 €
A new clinical trial
International clinical trial, Finland as reporting member state
The application concerns parts I and II (processing at the same time) 10 300€ /10 600 € ATMP-product
The application concerns part I (processing separately) 7 300 € /7 600 € ATMP-product
The application concerns part II (processing separately) 3 200 €
International clinical trial, Finland as a concerned member state (either in connection with the evaluation of the original application or when Finland is added as a concerned member state)
The application concerns parts I and II (processing at the same time) 7 500 € /7 800 € ATMP-product
The application concerns part I (processing separately) 4 500 € /4 800 € ATMP-product
The application concerns part II (processing separately) 3 200 €
National clinical trial, Finland as the reporting member state
The application concerns parts I and II (processing at the same time) 8 900 € /9 200 € ATMP-product
The application concerns part I (processing separately) 6 000 € /6 200 € ATMP-product
The application concerns part II (processing separately) 3 200 €
Adding a new member state
Adding a new member state, Finland as the reporting member state
The application concerns the addition of an EU member state as a new concerned member state, parts I and II at the same time 1000 €
Applications for modifications to clinical trials
Modification in international clinical trial, Finland as a reporting member state
Applications for modifications concerns parts I and II (processing at the same time) 3 300 €
Applications for modifications concerns part I (processing separately) 2 200 €
Applications for modifications concerns part II (processing separately) 1 300 €
Modification in international clinical trial, Finland as the concerned member state
Applications for modifications concerns parts I and II (processing at the same time) 2 500 €
Applications for modifications concerns part I (processing separately) 1 400 €
Applications for modifications concerns part II (processing separately) 1 300 €
Transition application from research under the directive to compliance with EU regulation
The application concerns parts I and II (processing at the same time) 500€
Evaluation of the annual report
Evaluation of the annual report 1000€