Charoon brings over 15 years of experience in Quality Management and Regulatory Affairs within the medical device industry. Her expertise includes the establishment and continuous development of ISO 13485-compliant quality management systems, as well as ensuring compliance with regulatory requirements for innovative medical devices.
At IKIM, she coordinates the development and implementation of quality- and regulatory-related frameworks for Software as a Medical Device (SaMD) throughout the entire development process. Working closely with interdisciplinary research teams, she supports the safe and regulatory-compliant transfer of innovative research into clinical practice.
