The Norwegian Medicines Agency (Statens legemiddelverk, Legemiddelverket) is the national regulatory authority in Norway for new and existing medicines and the supply chain. The Agency is responsible for supervising the production, trials and marketing of medicines. It approves medicines and monitors their use, and ensures cost-efficient, effective and well-documented use of medicines. The inspectorate also supervises the supply-chain and regulates prices and trade conditions for pharmacies.[1]
References
[edit]- ^ "Our goals and tasks". Norwegian Medicines Agency. Archived from the original on 2023-11-07. Retrieved 2023-11-07.