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What is a medicine?
Generic substitution
Generic products
Frequently asked questions
What is a biosimilar?
Frequently asked questions about biological drugs and biosimilars
What is a food supplement?
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Monitoring the safety of medicinal products
Adverse reactions
Submitting a report on an adverse reaction
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Ensure the safety of your medication
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Monitor the effects of your medication
How to store medicines?
How should medicines be disposed of?
List of medicines
Where can I find reliable information about medicines?
How can I assess the reliability of drug information?
Medicinal product packs
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How are medicines supplied to users in Finland?
What factors affect the availability of medicines?
Why might a pharmacy run out of my medicine?
Obligatory storing of medicines
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Why is the food supplement I ordered considered to be a medicine?
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What medicines can I bring abroad?
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Influenza
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Information for medicine users
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National medicines data repository
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Frequently asked questions (COVID-19)
Adverse reactions reported on corona vaccines
Russian attack on Ukraine
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Significant Polypharmacy in the Elderly
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Medicines Barometer
Marketing authorisations
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Finland as a Reference Member State in the decentralised procedure (DCP)
Finland as a Reference Member State in the Mutual Recognition / Repeat Use Procedure (MRP/RUP)
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Biological Medicinal Products
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Translating influenza vaccines in Finland
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Special characteristics of the electronic marketing authorisation process for veterinary medicines
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What are medical devices?
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Pharmaceutical safety and information
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Biological medicinal products
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Biosimilars
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The position of Fimea towards interchangeability of biosimilars
Regulation on Medicinal Products for Paediatric Use
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Coordination and communication
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Symbol in the labels of medicinal products
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Frequently Asked Questions
Manufacturing medicinal products
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PIC/S GMP Guide
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Frequently asked questions about reporting adverse drug reactions (ADRs)
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Narcotics control
Additional information to be submitted with narcotics licence applications
Frequently asked questions
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Gene technology register
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To users of the Pharmacopoeia
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Administrative regulations and guidelines
Blood services
Licence of a Blood Establishment
Hospital Blood Banks
Hemovigilance
Blood as a starting material for medicines
Legislation on blood service activities
Biobanks
National biobank register
Guidance and supervision of biobanks at Fimea
Tissue establishments
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Tissue establishment register
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Instructions for tissue establishments
Supervision of cybersecurity and resilience
Cybersecurity
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Frequently asked questions
Veterinary
Marketing authorisation procedures
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Mutual recognition procedure
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Validity of marketing authorisations
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Special permits for compassionate use
Applying for special permit
FAQ
A Questions and answers on how to fill in the form
B Questions and answers regarding the technical aspects of permit application
C Questions and answers regarding the decision and the processing of the application
D Other questions and answers
List of special permits for veterinary medicinal products
Adverse effects
Consumption of veterinary antimicrobials
The European Surveillance of Veterinary Antimicrobial Consumption ESVAC
Clinical trials on veterinary medicinal products
Immunological products
Withdrawal period and MRL
What is a withdrawal period?
MRL
Horses as food-producing animals
Private import
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Tabu: Regulations, Standards and Recommendations
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