Charoon Samerpark
Team Lead Regulatory Affairs
Institute for AI in Medicine, Germany
Charoon has more than 15 years of experience in quality management and regulatory affairs in the medical device field. Her work focuses on regulatory compliance and quality management systems for innovative medical technologies. At IKIM, she supports the development and regulatory approval of AI-based software as medical devices by establishing quality management processes and working closely with interdisciplinary teams to promote safe, responsible, and sustainable innovation in medicine.