Rebekka studied dentistry at Heinrich-Heine-University in Düsseldorf. After working as a dentist for several years, she moved to the private sector, where she gained in-depth regulatory expertise working within the dental medical device industry.
At IKIM, as a Regulatory Affairs Manager, Rebekka is co-responsible for the development and implementation of regulatory strategies for software as a medical device, as well as the establishment of Quality Management System processes in accordance with ISO 13485. The overarching goal of her work is to ensure regulatory compliance and product safety. By aligning software development with legal frameworks, she supports the IKIM ecosystem in transferring research directly into clinical application.
