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legemiddelverket.no

Norway’s medicines and medical devices authority regulates product safety, access, use and supply preparedness

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About legemiddelverket.no

Direktoratet for medisinske produkter (DMP) is Norway’s national authority for medicines and medical devices. It works to support timely and equitable access to effective products, monitor safety, promote appropriate use, and contribute to research and innovation.

DMP advises healthcare services, businesses and academia, and oversees areas including product development and production, sales, clinical trials, adverse-event reporting and medical-device registration.

Product: Regulatory oversight, guidance and safety monitoring for medicines and medical devices.

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Website detection does not establish a paid subscription or company-wide use. Tools loaded after consent or sign-in may be missed. “No longer observed” does not prove the company stopped using a tool.