HirLan, Your Human Factors Partner

Your Partner

HirLan partners with medical device manufacturers to assist with Human Factors Engineering through product innovation, development, evaluation (formative)/validation(summative) 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)/CE Mark Human Factors Requirements and comply with IEC 62366-1:2015 and ANSI/AAMI HE75:2009(R)2013 Human Factors Specifications. Our services include on-site business process consulting, on-site training, international seminars/workshops and Human Factors evaluation (formative) and validation (summative) 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) / CE Mark Human Factors Guidance.

Our Key Methods include:
  • Usability Testing
  • Iterative Design and Testing Methods
  • Human Factors Design Best Practices
  • Human Factors Training/Education
  • User Centered Participatory Design Methods
  • Innovation Process Methods
  • Business Process Consulting