Regulatory Compliance Expert in the Medical Devices Sector 💡 🌍 I am passionate about the development of the HealthTech sector, where innovative technologies meet regulatory and systemic requirements. On a daily basis, I work on ensuring medical devices comply with applicable legal regulations, particularly Regulation (EU) 2017/745 (MDR) and harmonized standards. I am eager to take on challenges that require a holistic approach — from regulatory requirements analysis, through building and improving management systems, to providing practical support for project and operational teams. I value solutions based on risk analysis, continuous improvement, and interdisciplinary collaboration that genuinely foster innovation in healthcare. 🔗 Feel free to connect and collaborate!