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Licensing and supervision
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Licensing of medicines
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Report suspected illegal activities
Falsified medicines
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Medicinal Products Committee
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Side effects and product information
Side effects and product information
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Additional monitoring
News on pharmacovigilance
Biological and biosimilar medicinal products
Safety updates
Post Authorisation Safety Study
Direct Healthcare Professional Communication
Adverse events
Drug interaction
Pharmacovigilance Council
Find medicines
Publications
Reimbursement and prices
Reimbursement and prices
General reimbursement
Individual reimbursement
Calculate reimbursement
Medicines bought in another EU/EEA country
Reimbursement Committee
Prices of medicines
Product numbers
Central Reimbursement Register
Reimbursable nutritional products
Publications
Pharmacies and sale of medicines
Pharmacies and sale of medicines
Pharmacies
Sale outside pharmacies
Over-the-counter medicines
Substitution
Medicines imported from abroad
Buying and selling medicines online
Sale of medicines or food supplements online
Doctors buying medicines for use in their own practices
Report suspected illegal sale of medicines
Prescriptions from another country
Publications
Medical devices
Medical devices
New regulations
COVID-19 antigen test for self-test
Advice to consumers on buying face masks
New Tech – new technological possibilities and medical devices
Patient safety and safe medical devices
Development of medical devices
Regulatory advice for medical device companies
CE marking
Incident reporting
Notified bodies
Registration and marketing
Clinical investigations
Performance studies of in vitro diagnostic medical devices (IVDs)
Certificates of Free Sale
Legislation and guidance
Publications
Special product areas
Special product areas
Veterinary medicines
Natural medicinal products and vitamin and mineral products
Euphoriant substances
Medical gases
Radiopharmaceuticals
Medicines affecting the ability to drive
Medicinal cannabis
Regulation of innovative medicinal products including ATMP
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Click here to see the Danish page 'Fra december 2022 skal alle sponsorer for kliniske forsøg med lægemidler registreres i den europæiske database EudraVigilance for fremover at kunne indberette alvorlige uventede bivirkninger (SUSARs)'
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