BE-GY 9763
Regulatory Issues Surrounding Medical Devices
Medical devices are developed, manufactured, and distributed in a highly regulated environment. This course primarily concerns the processes for obtaining FDA marketing approval or clearance for biomedical devices. Prior to marketing a medical device in the US, a specific governmental approval or clearance is required depending on the type of device and the risk associated with the device. | Prerequisite: Instructor and adviser's approval.
Sources
- Course catalogue ↗2026-2027