Ivo Flipse

Ivo Flipse brings extensive experience in the medical device industry, with a strong focus on Quality Management Systems, Regulatory Affairs, and operational excellence. Throughout his career, he has supported medical device manufacturers in navigating complex regulatory requirements, strengthening quality processes, and achieving compliance across international markets. His expertise spans product development, certification, and post-market activities, helping organisations translate regulatory expectations into practical, sustainable solutions. Through his blogs, Ivo shares practical insights and industry perspectives to help readers better understand the evolving medical device regulatory landscape.