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What is a biosimilar?
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Frequently asked questions about biological drugs and biosimilars
What is a food supplement?
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Monitoring the safety of medicinal products
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Ensure the safety of your medication
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List of medicines
Where can I find reliable information about medicines?
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How can I assess the reliability of drug information?
Medicinal product packs
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How are medicines supplied to users in Finland?
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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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Russian attack on Ukraine
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Meds75+
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Frequently asked questions
National High-Risk Medicines Classification
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Frequently asked questions
Consumption
Self-medication products
Basic register
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Plasma-derived products with marketing authorisation
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Assessment of pharmacotherapies (HTA)
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Assessment of hospital-only medicinal products
Topic selection
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National Medicines Information Network
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Medication Therapy Indicators
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Use of Avoidable Medications in the Elderly
Significant Polypharmacy in the Elderly
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Research Network for Rational Pharmacotherapy (RATTI)
Marketing authorisations
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Marketing authorisation application
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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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Translating influenza vaccines in Finland
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Special characteristics of the electronic marketing authorisation process for veterinary medicines
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Exemption
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Herbal medicinal products
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Cancelling a marketing authorisation or registration
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What are medical devices?
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Pharmaceutical safety
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Biological medicinal products
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Advanced Therapy Medicinal Products
Biosimilars
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Biosimilars in Finland
The position of Fimea towards interchangeability of biosimilars
Regulation on Medicinal Products for Paediatric Use
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Good Laboratory Practice (GLP)
Obligatory storing of medicines
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List of products to be stocked as obligatory storage
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Supervising tissue establishments
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Certificates of a Pharmaceutical Product (CPP)
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Additional information to be submitted with narcotics licence applications
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Batch-specific control
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National and international collaboration
Legislation, regulations and guidelines
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European Pharmacopoeia
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National pharmacopoeia documents
To users of the Pharmacopoeia
CEP Procedure
International Non-proprietary Names for Pharmaceutical Substances (INN)
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Blood services
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Licence of a Blood Establishment
Hospital Blood Banks
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Blood as a starting material for medicines
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Biobanks
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Biobank consent
National biobank register
Guidance and supervision of biobanks at Fimea
Tissue establishments
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Licence for tissue establishment
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Marketing authorisation procedures
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Special permits for compassionate use
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Applying for special permit
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List of special permits for veterinary medicinal products
Adverse effects
Consumption of veterinary antimicrobials
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The European Surveillance of Veterinary Antimicrobial Consumption ESVAC
Clinical trials on veterinary medicinal products
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Immunological products
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Fimea Sustainability Report 2023
Fimea Sustainability Report 2023
Director General’s review and Fimea’s sustainability policies
Promoting access to medicines and medical products
Safe medicinal treatment of production animals, environmental protection and reduction of national drug wastage
Supporting innovation and development of infrastructure
Safety of medicines and medicinal products and production of reliable medicines information
Fimea’s footprint – social, ecological and economic responsibility
Fimea Sustainability Report 2022
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Promoting access to medicines and medical products
Safe medicinal treatment of production animals, environmental protection and reduction of national drug wastage
Supporting innovation and development of infrastructure
Safety of medicines and medicinal products and production of reliable medicines information
Fimea’s footprint – social, ecological and economic responsibility
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