With years of dedication to the healthcare sector, I’ve developed a deep passion for ensuring the safety and compliance of pharmaceutical products. My journey in pharmacovigilance, regulatory compliance, and quality improvements has taken me across diverse markets, from the EU/UK to SEA, South Africa, LATAM, CIS, and MENA.

I take pride in leading clinical trials, preparing regulatory dossiers, and supporting post-marketing activities, all while conducting audits and trainings that uphold industry standards. My work spans diverse product types, including chemical entities, biological products, advanced therapy medicinal products (ATMPs), generics, and biosimilars.

Whether it’s navigating complex challenges or helping organizations achieve their project goals, I’m here to provide professional expertise and strategic guidance every step of the way