Hrvatski Home Medicines Verification Medicines Verification NMVO/NMVS EMVO/EMVS Falsified Medicines Patient Safety Alerts Stakeholders Stakeholders MA Holders Pharmacies & Hospitals Wholesalers IT Software Providers News Information Information Legislation Governance FAQ Useful Links CMVO About HOPAL What We Do HOPAL Service Provider Funding Information——— Home › Information › Legislation Information Legislation Governance Frequently Asked Questions Useful Links Legislation —— Directive 2011/62/EU of the European Parliament and of the Council of 8 June 2011 amending Directive 2001/83/EC on the Community code relating to medicinal products for human use, as regards the prevention of the entry into the legal supply chain of falsified medicinal products Commission Delegated Regulation (EU) 2016/161 of 2 October 2015 supplementing Directive 2001/83/EC of the European Parliament and of the Council by laying down detailed rules for the safety features appearing on the packaging of medicinal products for human use Zakon o lijekovima Republike Hrvatske (NN 76/13) Zakon o izmjenama i dopunama Zakona o lijekovima (NN 100/18) © 2025 HOPAL Croatian Medicines Veryfication Organization Radnička 80, 10000 Zagreb, Croatia T +385 (0)1 5625 759 E *protected email*
