End-to-End Cycle of Medical Device Design and Development

Learn the complete lifecycle of medical device design and development in this 57-minute lecture by Daniel Christadoss from Saint Louis University's Aerospace & Mechanical Engineering department. Explore the comprehensive process from initial concept through final product delivery, covering regulatory requirements, design controls, risk management, and validation procedures essential for bringing medical devices to market. Gain insights into industry best practices, FDA compliance standards, and the critical phases of medical device development including needs assessment, design inputs and outputs, verification and validation testing, and post-market surveillance. Understand the interdisciplinary approach required for successful medical device innovation, incorporating engineering principles, clinical requirements, and regulatory frameworks that govern the medical device industry.