has over 9 years of experience in the medical device industry. After successfully graduating with a degree in electrical engineering and information technology, he worked as a software engineer for a medical device manufacturer of high-risk products. Since 2016, he has been working at CE plus GmbH and is responsible for regulatory affairs in the area of active medical devices/medical software. He supports customers in the strategic and practical implementation of regulatory requirements in the context of CE marking. He has versatile experience in the establishment and implementation of the software life cycle process according to IEC 62304 and the creation of technical documentation. He is also a member of various standardisation committees on medical software and information security in medical technology.