Explore the human side of device design and learn to develop safe and effective systems that can help a wide range of people in a variety of settings. Study how government oversight, U.S. and international laws, clinical strategies, quality assurance and regulations influence and control the creation and production of medical devices. Gain practical tools and strategic methods for successfully commercializing new products. Understand patents, copyrights, U.S. and international laws, and regulatory and clinical strategies, including quality assurance and inspection.
Key Outcomes
You will know the complete process for safe medical device development.