Sabrina is Regulatory Affairs Manager at SFL.

She leads regulatory projects, providing support to SFL clients for the development, filing, and maintenance of healthcare products such as medical devices, IVDs and combination products.

Sabrina is involved in the preparation, review and submission of high-quality regulatory documentation for medical devices, IVDs and combination products.  Based on her deep understanding of technical data and regulatory processes she develops documents specifically tailored to SFL clients’ needs and products. This notably includes scientific advice briefing booklets, risk assessments, quality and technical documentation.

Before joining SFL, Sabrina held various roles with increasing responsibilities in diagnostics and pharmaceutical industry. During her previous roles she has gained extensive knowledge and hands-on experience on strategical and operational aspects of medical devices and IVDs.

She holds a Master of Science in Life Sciences from the University of Applied Sciences FHNW in Switzerland.