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Responsible for the service Finnish Medicines Agency Fimea

Manufacturing license for a pharmaceutical company

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  • When applying for a licence for the industrial manufacture of medicinal products or the manufacture of medicinal products for clinical trials, the applicant shall submit to Fimea’s registrar’s office a free-form licence application including the documents and details listed in section 1 of the Medicines Decree. When applying for a licence pursuant to section 15a of the Medicines Act, administrat ...

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Text edited by: Finnish Medicines Agency Fimea
Updated: 13/11/2025