Implement the New
FDA 510(k) Human Factors Guidance

Meetings

There has been a lot of talk and some confusion about implementing the FDA 510(k) Human Factors Guidance.

Join us for breakfast. We will introduce you to the FDA 510(k) Human Factors Guidance and the ANSI/AAMI HE75:2009(R)2013 Human Factors Engineering-Design Specifications as they relate to medical devices and medical related software. You will walk away with a better understanding of the impact these requirements have on your product lifecycle and related product release schedule. Click on a meeting below for more information.

Breakfast Meeting Breakfast Meeting - La Jolla, CA   March 13, 2013 8:00am
An Introduction to the FDA 510(k) Human Factors Guidance