Lægemiddelstyrelsen
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About
Lægemiddelstyrelsen is the Danish Medicines Agency, the national regulatory authority responsible for medicines and medical device oversight in Denmark. Its responsibilities include approval and control of medicines, clinical trial oversight, pharmacovigilance (adverse reaction reporting and safety updates), manufacturer and device registration and inspection, distribution and pharmacy regulation, subsidy and pricing information, issuing export and distribution certificates, guidance on medical devices (including CE marking and clinical performance investigation), and public information for citizens, healthcare professionals and industry.
Sector
Health Care
Industry Group
Health Care Equipment & Services
Industry
Health Care Providers & Services
Subindustry
Health Care Services
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