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.