Developing a medical device in compliance with ISO 13485 and Regulation (EU) 2017/745 (MDR) requires a structured approach from the earliest stages. In this webinar in collaboration with COESUM, we will explore the main milestones of the journey from concept to product, with a focus on the European regulatory framework, design and development, change management, and the selection of appropriate materials and processes. This session is designed to provide a clear and practical overview of the key stages, helping companies and professionals avoid mistakes and delays in the development process.