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EU Falsified Medicines Legislation – Update

14 February, 2019

The European Commission’s Delegated Regulation on safety features for medicinal products for human use comes into operation across Europe from 9 February 2019.

The Falsified Medicines Directive has been updated and is in force from the 9th February in a "use and learn" phase.

This new medicines’ verification system is a significant undertaking involving the collaboration of almost 2,000 pharmacies and hospitals, along with pharmaceutical manufacturers and wholesalers, stakeholder representatives and regulators, which sees over 95 million prescription medicines dispensed to patients every year.

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