Claudia Brilli

Claudia Brilli has extensive experience in the field of regulatory affairs and quality compliance within the medical device sector, specifically for ophthalmic applications. Since November 2013, Claudia has been part of FARMIGEA's Regulatory Affairs department, focusing on the preparation, maintenance, and updating of technical documentation related to CE marking in accordance with EU regulations. Prior to this role, Claudia served as a Laboratory Analyst at FARMIGEA Holding s.r.l. from September 2011 to September 2013, where responsibilities included quality control and completing a thesis internship on pharmacokinetics and pharmacodynamics of a new ophthalmic preparation. Earlier experience includes a laboratory analyst internship in biological quality control at FARMIGEA Holding s.r.l. Claudia holds a Laurea Magistrale in cellular and molecular biology and a Laurea Triennale in biological sciences, both from the Università di Pisa.