Ana González-Lamuño Rubiera advises clients in the pharmaceutical, biotechnology and medical devices sectors on a broad range of EU Regulatory matters. She assists them throughout the lifecycle of their products, including clinical investigations, product classification, authorization, pharmacovigilance, marketing and promotional activities, and privacy and data protection.
Prior to joining the firm, Ana worked in the EU Life Sciences department of a leading international law firm in Brussels, and completed a traineeship at the Cabinet of the President of the General Court of the European Union in Luxembourg.
Ana is fluent in French and English, and is a native Spanish speaker.
- LL.M., European Legal Studies, College of Europe, 2021
- LL.B., Law, Universidad de Cantabria, 2015
- Brussels, Belgium (E-list)