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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?
Safety of medicines
Monitoring the safety of medicinal products
Adverse reactions
Submitting a report on an adverse reaction
Medicinal products under additional monitoring
Product defects
Drug interactions
Pharmaceutical injuries
Correct use of medicines
Ensure the safety of your medication
Instructions for the safe use of medicines
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
Package leaflet
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
Exemptions and special permits
Ordering medicines online
Why is the food supplement I ordered considered to be a medicine?
Medicines for children
Developing better medicines for children
Collaboration on medicines education
Medication of the elderly
What medicines can I bring abroad?
Pain relievers and self-care
Bringing medicines to Finland
Fimea’s services to citizens
Cooperation with patient associations
Influenza
Influenza vaccinations
Antiviral medication
Pandemic
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Falsified medicines
Medicines and pregnancy
Pharmaceuticals and the environment
Antimicrobial resistance
Medicines that have marketing authorisation in Finland
Current events
Retail sale of non-prescription medicines
Support and guidance for retail stores
Retail store responsibilities
Retail sale of non-prescription medicines – FAQ
Substitution of biological medicines
Information for medicine users
Information for health care professionals
Farmasto
Fimea and wellbeing services counties
Coronavirus (COVID-19)
Adverse reactions reported on corona vaccines
Russian attack on Ukraine
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Meds75+
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National High-Risk Medicines Classification
Frequently asked questions
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Topic selection
Nordic collaboration through JNHB
Assessment reports (in Finnish)
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Medication Therapy Indicators
Use of Avoidable Medications in the Elderly
Excessive Polypharmacy in the Elderly
Drug Expenses for the Elderly
Patient advisory board
Research
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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)
Changing of Reference Member State duties to Finland
Finland as a rapporteur in the centralised marketing authorisation procedure (CP)
Granted and cancelled marketing authorisations
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Biological Medicinal Products
Orphan drugs
Paediatric medicines
European Pharmacopoeia
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Renewals
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Product Information
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Translating influenza vaccines in Finland
Electronic marketing authorisation submissions
What's new
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Special characteristics of the electronic marketing authorisation process for veterinary medicines
Introduction to market
Shortage notifications
Frequently asked questions about reporting shortages
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Frequently asked questions about marketing authorisations
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What are medical devices?
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Medical Device Advisory Clinic
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Notified bodies
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Devices subject to specific additional procedures
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Pharmaceutical safety and information
Pharmaceutical safety
Reporting adverse reactions
Biological medicinal products
Advanced Therapy Medicinal Products
Plasma-derived products
Biosimilars
Biosimilars in Finland
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
Pharmacies
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Special permits
Applying for a special permit – Information for prescribers
Applying for a special permit – Information for the releasing party
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Search for medicinal products requiring a special permit
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Granted Exemptions (Nordic flex EN/EN packages)
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New regulation on substances of human origin
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Biobanks
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Supervision
Pharmacovigilance
Adverse reaction reporting (EudraVigilance)
Frequently asked questions about reporting adverse drug reactions (ADRs)
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Clinical Drug Trials
Clinical Trials Regulation & CTIS
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Supervision of pharmaceutical marketing
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Classification
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Good Laboratory Practice (GLP)
Obligatory storing of medicines
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Applying for an exemption
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Certificates of a Pharmaceutical Product (CPP)
Applying for an export certificate
Narcotics control
Frequently asked questions
Batch-specific control
GMP certificates
Gene technology
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European Pharmacopoeia
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International Nonproprietary Names for Pharmaceutical Substances (INN)
Additional Pharmacopoeia materials
Administrative regulations and guidelines
Cybersecurity
Frequently asked questions
Assessment tool for the Cybersecurity Act
Resilience of critical entities
Veterinary
Marketing authorisation procedures
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Mutual recognition procedure
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Centralised procedure
Validity of marketing authorisations
Applications for variations to marketing authorisations for veterinary medicines
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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