PGF Pharma International

Our core service is regulatory, and as experts in the field, we’re constantly called on to explain how international drug registration functions and why it has to be so complicated.

Over the years, we’ve learned that regulatory projects require due diligence from start to finish. Due to their significant workload—often within a short period of time—immediate action is essential to successfully processing license applications.

Based in Croatia, we are also specialists in the EU and South East European market and can assist you in assessing this specific market if this is your single need.

While we specialize in regulatory, we also provide services in all related areas, ensuring that our clients obtain market access with an appropriate price and reimbursement level. In short, we strive to optimize all aspects of development.