I am passionate about making complex regulatory requirements understandable, and helping developers of medical devices establish processes that ensure compliance with the requirements, taking into account agile thinking and limited resources.

With more than 20 years in software development, with practical experience at all levels combined with deep insight into regulatory requirements and compliance processes for medical devices combined with solid business understanding, I contribute at WHINN with insight and understanding of both the regulatory requirements, the practical implementation of processes and documentation as well as the business, and the balance between these.