Pharmaceutical professional and scientific leader with over 20 years of experience across the healthcare, regulatory, and clinical/pre-clinical research landscape. I currently serve as Deputy Director and GLP Officer at a GLP-certified spin-off CRO, i co-founded and lead. Our current work focuses on toxicological evaluation and regulatory compliance of medical devices, cosmetics, and topical pharmaceuticals.
My background bridges deep scientific knowledge, GLP regulatory standards, and operational CRO management. I’ve led pre-clinical studies under OECD GLP principles, supervised quality systems, and contributed to the design and submission of regulatory documentation for various product classes.
Beyond research and regulation, I also serve as a scientific advisor and contributor to the Panhellenic Pharmaceutical Association (PFS), with responsibilities that include:
• Authoring national and pan-European position papers on health policy and pharmaceutical care
• Designing and delivering educational programs for pharmacists and healthcare professionals
• Representing scientific perspectives in policy discussions at the institutional level
I am also a recognized peer reviewer for leading journals (Elsevier, Wiley, MDPI, Springer and Taylor & Francis).
Peer-Reviewed Articles in PubMedPeer-Reviewed Articles in PubMed
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