Marketing Authorisation Holders, Manufacturers, Wholesalers and those supplying medicines to the public will need to scan medicines at different points in the supply chain to introduce them into the repository, verify their authenticity and decommission them from the database at the time of dispense.
Further information regarding the obligations of each stakeholder in the supply chain can be found:
– in the document Letter to stakeholders regarding the implementation of safety features under the Falsified Medicines Directive 2011/62/EU
– on the web-page of the European Medicines Verification Organisation
– on our web-page