our story

Your Bridge to the EU Pharmaceutical Market: From Initial Guidance to Full-Scale Launch

Our Story:

Understanding Your Challenges, Delivering Real Solutions

PGF Pharma International’s journey began in Vietnam, where we provided EU-GMP consulting to Asian pharmaceutical manufacturers. We quickly learned that navigating the EU market was far more challenging than simply meeting regulations.
We saw firsthand the hurdles you face: complex approvals, strict compliance, and the intricacies of building European partnerships. It became clear that you needed more than just advice – you needed a partner to handle every step of the process.

PGF’s Evolution:

Your Complete EU Market Entry Partner

 

That’s why PGF Pharma expanded. We transformed from consultants into your dedicated partner for a successful EU launch. We now provide a comprehensive suite of services designed to make your market entry effortless:

  • Effortless EU Market Access: We handle all regulatory compliance and market authorization requirements.
  • Uncompromising Quality: Expert batch release, quality assurance, and pharmacovigilance services.
  • Strategic Market Success: Proven commercialization, distribution, and market access strategies.

With our headquarters in Croatia and a strong European network, we provide the expertise and connections you need to thrive in the EU market.

vision, MISSION

Leadership

Meet Our Leadership & Expert Team
At PGF Pharma International, our strength lies in our people. Our leadership and specialist teams combine decades of pharmaceutical industry experience with deep functional expertise and a commitment to quality, compliance, and client success.

Josipa FriSCiC BenkoviC

CEO and Head of Regulatory Affairs

Pharmacist with 20 years’ industry expertise in Regulatory Affairs & Pharmacovigilance. As CEO, she drives excellence, ensures regulatory integrity, and leads PGF’s sustainable growth.

Marko MoriC

Co-founder & Director of Asian Markets

Co-founder with 20+ years’ experience in Asia, specializing in business development, government relations, and geopolitical strategy. Leads Asian market engagement, leveraging strong networks and cross-border partnership success.

Goran ReSiC

Co-founder & Director of Sales and Procurement

Co-founder with extensive pharmaceutical business development experience. Established PGF’s mission for high-quality solutions and drove growth through strategic sales and procurement leadership.

Antonia Ravlija

Quality Associate

Chemical Engineer with 2 years’ pharmaceutical/food industry experience, applying analytical skills to uphold EU GMP standards, manage quality documentation, and support robust QA processes.

Mauro KalCiC

Business Development and Sales Specialist

8 years of pharmaceutical experience specializing in API/FDF trade. Skilled in market analysis, international negotiation, identifying opportunities, and forging strategic partnerships to drive business growth.

Tina SoStariC

Head of Quality

Pharmacist and Qualified Person (QP) with 20+ years of leadership in Quality & Production (Sterile/Semisolid). Proven success driving strategic initiatives, major capital projects, implementing EU Annex 1, and delivering operational excellence via lean methods.

Branka VuCkoviC

Regulatory Specialist

Brings 19 years’ pharmaceutical experience (10 in Quality/Stability, 9 in Regulatory Affairs with EU focus). Applies extensive knowledge to ensure regulatory compliance and guide product registration.

Martina StojiC

Regulatory Specialist

Chemist with 3 years of prior administrative experience, now focusing on ensuring regulatory compliance, preparing registration documentation, and supporting cross-functional teams in meeting international requirements.

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Mia Korotaj

Head of Quality Control

With a Ph.D. in Analytical Chemistry and extensive experience in GMP compliance and quality systems, Mia is dedicated to driving quality and innovation in pharmaceutical processes.

Certifications and Compliance

Certification & Compliance: Meeting the Highest EU Standards

PGF Pharma International operates under the strictest regulatory standards, ensuring full compliance with EU pharmaceutical laws. As a licensed EU-GMP (Good Manufacturing Practice) manufacturer, our operations are backed by essential certifications that underscore our commitment to quality, safety, and regulatory excellence:

  • Manufacturing and Import Authorization (MIA)
  • Good Distribution Practice (GDP) License
  • API (Active Pharmaceutical Ingredient) Trade License
  • Medical Device License

These credentials authorize us to manage manufacturing, importation, distribution, and commercialization activities throughout the EU market comprehensively.