Medicines Verification System
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Alerts
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Pursuant to the provisions of the Commission Delegated Regulation (EU) 2016/161, at the point of dispense the medicine will be scanned, checked and verified for authenticity against a national (or EU) repository. If the UI on the pack matches the information in the repository, the pack is decommissioned and supplied to the patient. Otherwise, if there is a warning related to this pack, then the system will highlight this as an exceptional event and the package will not be supplied to the patient. An investigation needs to determine whether the pack has been falsified or not.

Please find detailed information regarding alert handling in the Guidelines for EMVO and NMVO stakeholders.

Letter to stakeholders

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).

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Amount of the annual fee

HOPAL determined the amount of the annual fee for the Croatian Medicines Verification System usage by MAHs
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About HOPAL

The Croatian Medicines Verification Organisation (HOPAL) is a non-profit organisation representing the different stakeholders, both...
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© 2018 HOPAL

Croatian Medicines Veryfication Organization
Radnička 80, 10000 Zagreb, Croatia
T +385 (0)1 5625 759
F +385 (0)1 5625 760
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