Learn About Human Factors

About Human Factors

MDHF partners with medical device manufacturers to assist with Human Factors Engineering through product innovation, development, validation/evaluation testing, and delivery. We specialize in the custom integration of Human Factors Best Practices into your specific product and business processes environment to meet the FDA 510(k) Human Factors Guidance and the ANSI/AAMI HE75:2009(R)2013 Human Factors Engineering-Design of Medical Devices. Our services include on-site business process consulting, on-site training, international seminars/workshops and Human Factors evaluation and validation testing.

Incorporating Human Factors principles into your product lifecycle will minimize your product development costs and time to market while delivering products with a strong competitive advantage. Our expertise will simplify the process of incorporating Human Factors principles into your business processes and product lifecycle and thereby satisfy the FDA 510(k) Human Factors Guidance.

Meetings — We offer International Comprehensive 3-Day Seminars/Workshops that provide tools, materials, and a comprehensive plan for you to get started with integrating Human Factors principles into your business processes and product lifecycle so you can comply with the FDA 510(k) Human Factors Guidance. You can register at: events.medicaldevicehumanfactors.com

3-Day Seminar/Workshop — We offer International Comprehensive 3-Day Seminars/Workshops that provide tools, materials, and a comprehensive plan for you to get started with integrating Human Factors principles into your business processes and product lifecycle.

Private Customized Workshops — We customize our 3-day seminar/workshop to your company’s business/development processes and product lifecycle. Upon completion of the workshop you will have a customized plan, which incorporates Human Factors principles into your product's business/development processes to comply with the FDA 510(k) Human Factors Guidance.