Evgenia Mengou has 30 years’ experience in the regulation of human medicines across global markets. She has worked on both small molecules and biologics, including vaccines, in diverse business and cultural settings, across a variety of therapeutic areas. She has held project leadership and management roles.
In 2016, she set up her own consultancy to provide clients agile regulatory expertise for the development and worldwide registration of medicines.
She was awarded Fellowship status by TOPRA in 2019.
She served on the TOPRA Board for two terms from 2020 - 2023. She is also a Trustee and Board member of aPODD, a philanthropic organisation focused on accelerating pediatric drug development, as well as a member of the ACCELERATE FAIR working group.
She has been a Guest Lecturer at University of Limerick’s Postgraduate Diploma in Regulatory Affairs.