About medical deviceshttps://helsedirektoratet.no/english/medical-devices/about-medical-devicesAbout medical devicesThe Norwegian Directorate of Health’s role regarding medical devices. Legislation related to medical devices. Legal interpretations.1683
Regulatory informationhttps://helsedirektoratet.no/english/medical-devices/regulatory-informationRegulatory informationMedical devices - Register. Clinical investigation. Classification. Placing on the market. Free sales certificate. Notified body. Administrative and advisory responsibilities related to legislation for medical devices.1684
Reporting of adverse incidents involving medical deviceshttps://helsedirektoratet.no/english/medical-devices/reporting-of-adverse-incidents-involving-medical-devicesReporting of adverse incidents involving medical devicesIncidents with medical devices on the market, as well as injuries, accidents and failures where medical devices is or may have been involved, shall be reported to the Norwegian Directorate of Health, department of medical devices and medicinal products.1695
Glossary – Medical deviceshttps://helsedirektoratet.no/english/medical-devices/glossary-medical-devicesGlossary – Medical devices1697

Sist faglig oppdatert: 1. september 2016

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