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Advertisinghttps://legemiddelverket.no/english/medical-devices/requirements-and-responsibilities-regarding-medical-devices-on-the-market/advertisingAdvertisingInformation regarding advertising for medical devices in Norway and limitations for which claims that can be used in advertising.3514Information regarding advertising for medical devices in Norway and limitations for which claims that can be used in advertising.
Cases in which obligations of manufacturers apply to importers, distributors or other personshttps://legemiddelverket.no/english/medical-devices/requirements-and-responsibilities-regarding-medical-devices-on-the-market/cases-in-which-obligations-of-manufacturers-apply-to-importers-distributors-or-other-personsCases in which obligations of manufacturers apply to importers, distributors or other personsImporters, distributors or other persons will, with article 16 of MDR and IVDR, have clearer requirements when carrying out changes to packaging to a device, repackaging or other changes to medical devices.3527Importers, distributors or other persons will, with article 16 of MDR and IVDR, have clearer requirements when carrying out changes to packaging to a device, repackaging or other changes to medical devices.
Distance Sales/Online sales/E-commercehttps://legemiddelverket.no/english/medical-devices/requirements-and-responsibilities-regarding-medical-devices-on-the-market/distance-salesonline-salese-commerceDistance Sales/Online sales/E-commerceInformation on the requirements that apply to medical devices for online sales, free samples and when importing for personal use.3498Information on the requirements that apply to medical devices for online sales, free samples and when importing for personal use.
Free Sales Certificate (English)https://legemiddelverket.no/english/medical-devices/requirements-and-responsibilities-regarding-medical-devices-on-the-market/free-sales-certificate-englishFree Sales Certificate (English)Free Sales Certificate to Norwegian manufacturers of medical devices. 1584
Market surveillance and auditing of medical deviceshttps://legemiddelverket.no/english/medical-devices/requirements-and-responsibilities-regarding-medical-devices-on-the-market/market-surveillance-and-auditing-of-medical-devicesMarket surveillance and auditing of medical devicesThe Norwegian Medicines Agency is the competent authority for medical devices in Norway. Auditing is one of the most important tools we have to ensure that medical devices that are placed on the market in Norway are safe and secure. 3500

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