Applying Human Factors and Usability Engineering to Medical Devices: Guidance for Industry and Food and Drug Administration Staff
Information
Type
Guidance
Regulated products
Medical Devices
Topics
Digital Health, Labeling, Microbiology, Postmarket, Premarket, Safety - Issues, Errors, And Problems
Published
February 3, 2016
Last updated
February 9, 2019
Description
This document provides guidance on applying human factors and usability engineering to medical devices for industry and FDA staff.
Tags
Organization
Country / Region
United States
License
Other (Public Domain)