3-Day Hands-On Workshop to Incorporate
the New FDA 510(k) Human Factors Guidance

Seminars/Workshops

How are you incorporating the new FDA 510(k) Human Factors Guidance and the ANSI/AAMI HE75:2009(R)2013 Human Factors Engineering-Design Specifications for medical devices into your products? Did you know these standards and guidelines are actually good business practices, that when embraced, will reap user acceptance, business, and financial rewards?

This 3-Day Seminar with hands-on workshops designed to illustrate how to apply and embrace the new FDA 510(k) Human Factors Guidance. You will walk away with vital tools to help you incorporate both the FDA 510(k) Human Factors Guidance and the ANSI/AAMI HE75:2009(R)2013 Human Factors Engineering-Design Specifications for medical devices into your product cycles.

Who Should Attend - These Seminar Workshops are designed for all participants in the product lifecycle from the earliest ideation phase through product marketing and sales/support. This includes quality, design and research and development engineers and managers; risk managers; as well as personnel from product marketing, regulatory affairs, quality assurance, clinical/medical affairs, sales and customer service.

To Register or Learn more about our 3-Day Seminars/Workshops, contact us at MDHF@Hirlan.com