Medicines Verification System
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.
If you have any questions or need some information, we will gladly communicate with you via or via the following contact form. To successfully reply to your message, please, fill out all contact form fields and enter the summation result into the 'captcha' field to protect against spam messages:
© 2018 HOPAL
Croatian Medicines Veryfication Organization
Radnička 80, 10000 Zagreb, Croatia
T +385 (0)1 5625 759
F +385 (0)1 5625 760