Meet Insuvia team
Leading Insuvia toward its long-term vision and strategic objectives by shaping strategy and driving sustainable growth. With more than 15 years of experience in pharmacovigilance and regulatory affairs, Donatas specializes in building compliant frameworks that help organizations meet global standards while achieving operational excellence.
Providing leadership to Insuvia’s operational teams while maintaining strong relationships with clients. With over 18 years of experience in Pharmacovigilance and Regulatory Affairs, Martynas brings deep expertise in compliance and safety systems. He has served as a Qualified Person for Pharmacovigilance (QPPV) and led the development of PV systems for some of the most renowned companies in the industry.
Martynas holds a degree in Pharmacy, combining scientific knowledge with operational excellence to deliver reliable and compliant solutions for clients.
Driving the company’s growth by identifying and securing new business opportunities and building long-lasting relationships with clients and partners. With more than 7 years of experience in the industry, he specializes in guiding organizations through the setup of compliant Regulatory Affairs and Pharmacovigilance processes, ensuring full adherence to global standards.
Jonas holds a Master’s degree in Business Administration and a Master’s degree in Pharmacy, combining strategic business insight with deep pharmaceutical expertise to deliver comprehensive solutions for clients.
Leading Insuvia’s Pharmacovigilance department and serving as EU-QPPV, Ada ensures compliance and patient safety across all processes. With nearly 10 years of experience in Pharmacovigilance, she has overseen the development and management of PV systems for a wide range of products throughout their life cycle.
Ada holds a PhD in Pharmacy, combining scientific depth with regulatory expertise to deliver robust and compliant solutions that safeguard patients and support organizational success.
Oversees regulatory projects, ensuring adherence to timelines, budgets, and compliance requirements. She holds a Master’s degree in Pharmacy and has nine years of experience in Regulatory Affairs across EU (including non-EU) and CIS regions, specializing in biologic and chemical medicinal products. Her expertise includes outsourcing model selection, seamless handovers, integration processes, and coordination of internal and external resources.
