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Licensing and supervision
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Licensing of medicines
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Licensing and supervision
Licensing and supervision
Brexit
Licensing of medicines
Authorisation procedures
Company authorisations and registrations
Supervision and inspection
Clinical trials
How to evaluate evidence of the efficacy of medicines
Evaluation of reviews
Report suspected illegal activities
Falsified medicines
Compassionate use
Medicine or not
Export certificates
Fees
Name/address changes
Professional relationships and financial support, applicable to healthcare professionals and specialists
Relationships with and financial support from companies
Medicinal Products Committee
Publications
Side effects and product information
Side effects and product information
Side effects of medicines
Additional monitoring
News on pharmacovigilance
Biological and biosimilar medicinal products
Safety updates
Post Authorisation Safety Study
Direct Healthcare Professional Communication
Adverse incidents with medicines
Drug interaction
Pharmacovigilance Council
Find medicines
Publications
Reimbursement and prices
Reimbursement and prices
General reimbursement
Individual reimbursement
Reimbursement thresholds
Medicines bought in another EU/EEA country
Reimbursement Committee
The EU HTA regulation
Prices of medicines
Product numbers
Central Reimbursement Register
Reimbursable nutritional products
Publications
Pharmacies and sale of medicines
Pharmacies and sale of medicines
Think before you buy
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
Danish Board for Health Apps
Incident reporting
Interruption or discontinuation of the supply of medical devices
New regulations
New Tech – new technological possibilities and medical devices
Development of medical devices
Regulatory advice for medical device companies
CE marking
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 'GE Healthcare informerer om fejl ved udstyret SIGNA, Briva & Optima MR systems, der kræver opdatering af software'
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