Marketing Authorization Holders

Information for Marketing Authorization Holders

Alert-Management Onboarding / Registration Registered Marketing Authorization Holders Fees Guidelines

For Marketing Authorization Holders

According to the falsified medicines directive, all manufacturers must implement the two safety features 2D data matrix and tamper evidence for all human prescription medicines unless the products are listed on the “white list” (Annex I of the Delegated Regulation (EU) 2016/161).

Nomvec is responsible of the day-to-day operations and further development of the e-verification database for pharmaceutical products in Norway, on behalf of the pharmaceutical industry in Norway.