Alice is Associate Director Regulatory Affairs at SFL.
She leads regulatory projects, providing support to SFL clients for the development, filing, and maintenance of healthcare products, as well as for effectively negotiating and liaising with responsible authorities.
Alice is involved in the preparation, review and submission of high-quality regulatory documentation for EMA, Swissmedic, and FDA for medicinal products as well as for medical devices. The documents and materials she develops are informed by her deep understanding of scientific/medical data and regulatory processes, and specifically tailored to SFL clients’ needs and products. They include scientific advice briefing booklets, orphan designation dossiers, pediatric investigation plans, and clinical evaluation reports.
Before joining SFL, Alice worked in academic research studying the signaling pathways involved in cancer development, including doctoral research at the Cancer Research UK London Research Institute and postdoctoral work at the University of Geneva, Switzerland.
She holds a PhD in Cell Biology from University College London, UK and is an alumna of the Ecole Normale Supérieure in Paris, France.