Human Factors & User Experience for Medical Device Design


Human Factors & User Experience for Medical Device Design is a conference dedicated to Engineering Device Safety and Development through Usability Testing and Risk Mitigation

Human Factors & User Experience for Medical Device Design covers topics such as:

  • Streamline strategies for risk management activities to improve overall device design
  • Leverage usability testing early in the product development cycle to ensure a successful validation process
  • Assess existing and forthcoming regulatory impacts to best meet compliance standards
  • Establish internal alignment between design and human factors teams to improve product development
  • Examine the European Medical Device Regulation (EU MDR) to provide clarity on transition timelines and expectations

Human Factors & User Experience for Medical Device Design brings together attendees with responsibilities in:

  • User Experience Design/ User Design
  • Human Factors/Human Factors Engineer(ing)
  • Industrial Design Design Controls/Engineer
  • Usability/User Experience/User Interface/UX/UI
  • Research & Development (R&D) Engineer
  • Product Development
  • Quality/Quality Control/Quality Assurance/Quality Engineer
  • Device Engineering
  • Regulatory Affairs

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Please, check the official conference website for possible changes, before you make any traveling arrangements

Prices are for evaluation only.

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