Andreas is a quality and regulatory specialist with extensive experience in the medical device industry. He has built, implemented, and optimized quality management systems and has led product certifications and regulatory submissions in compliance with FDA, MDR, and other international standards. His experience spans both established companies and start-ups, combining regulatory expertise with a practical, systems-driven approach rooted in his earlier work in software development and electronics design. Andreas joined Odne as Quality Manager to lead quality and regulatory efforts and support global market access.