Duration: 4 hours
In addition to providing an in-depth discussion of contemporary design and development principles and practices (and corresponding EU and FDA regulatory requirements), this approximately four-hour, self-paced course explores the essential relationships between risk management and design and development throughout the lifecycle of a medical device.
This course is designed for risk management professionals, engineers, quality and regulatory professionals, and others engaged in design and development throughout the lifecycle of a medical device, as well as those managing risk management and design and development of medical devices.
By the end of this course, you will be able to:
This course is important for medical device professionals, especially those who conduct or participate in design phases of any project and/or quality systems activities specific to design control.
By completing/passing this course, you will attain the Medical Device Certificate.
Cost: $599 (per completion)