Workshop 5: Medical Device Under Design Control

During the workshop, we aim to provide participants with a comprehensive understanding of design controls, drawing from hands-on experience in leading cross-functional teams through the end-to-end development lifecycle of medical devices. We will cover key aspects such as risk management, validation, verification, and documentation processes, ensuring attendees leave with actionable insights and practical tools to enhance their research. This will equip them with the knowledge and skills necessary to navigate the complex landscape of medical device development.