Human Factors for Medical Devices

October 15 - 17, 2018

Dun Laoghaire, Dublin

This 3-day course offers participants a comprehensive overview to human factors as it relates to medical devices. It includes regulatory requirements of FDA, specifically the interpretation from the Center for Devices and Radiological Health (CDRH) Human Factors Team, as they relate to human factors, and the process of applying human factors in design controls during the design of a medical device. The course also includes the regulatory perspective of the Center for Drug Evaluation and Research (CDER) and the impact of human factors on pharma.

More Information

Click here for a detailed overview—including program objectives, content, and schedule.

Learn More