Medicines Verification System
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Medicines Verification System
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A key measure to address falsification in the EU and protect the legal supply chain of medicines is an end-to-end verification system introduced by the Falsified Medicines Directive (FMD). The end-to-end verification is a medicines authentication system including mandatory safety features and a repository that stores information on each individual pack.

Further information regarding the Medicines Verification System 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