Giulia Girola

Giulia Girola is a Regulatory Affairs Specialist at Materialise in Leuven, Belgium, focusing on the orthopedic portfolio. She ensures regulatory compliance and market authorization for CE-marked and custom-made devices in the EU and FDA-cleared devices in the US by preparing and submitting technical documentation and collaborating with internal stakeholders and regulatory agencies.

Previously, Giulia worked at LimaCorporate S.p.A. in Italy, specializing in custom-made medical devices, where she gained experience in regulatory compliance across multiple regions. She holds a Master’s degree in Biomedical Engineering from Politecnico di Milano and completed an exchange program at Technische Universiteit Eindhoven.