Human Factors Usability Studies Following ISO 62366 and FDA Guidance

Duration: 60 Minutes
This training program will examine how human factors/usability is the analysis of how people interact with medical devices. The process of conducting rigorous human factors studies throughout the design process, integrating it with the device risk analysis and design process and validating the effectiveness of the studies will be explained. The various types and methods of human factors analysis will be explained. This process conforms to the new ISO 62366 standard and the new FDA guidance document.
ISO 62366 Training Program
Instructor: Edwin Waldbusser
Product ID: 509704
Objectives of the Presentation
  • User error versus use error
  • Use related hazards and risk analysis
  • User profiles
  • Use scenarios
  • Step by step human factors program development
  • Validation
Why Should you Attend
The FDA will only approve devices designed so that it is practically impossible for people to accidentally harm themselves even if they use the device improperly. The FDA has replaced the term "user error" with "use error," which means that it's how the product is used and not human error that is considered by the FDA to be a device nonconformity. As a result, human factors should be considered in the design process, and the burden is now on the device designer to create an "idiot proof" product.

Human Factors Usability Testing is the analysis of how people interact with medical devices. In this session, expert speaker Edwin Waldbusser will explain the process of conducting rigorous human factors studies throughout the design process, integrating it with the device risk analysis and design process, and validating the effectiveness of the studies. The various types and methods of human factors analysis will also be explained. This process conforms to the new ISO 62366 standard and the 2016 FDA guidance relating to it.

Areas Covered
  • The need for understanding and optimizing how people use and interact with technology
  • Definitions: Use scenario, task, critical task
  • 2016 FDA Guidance on applying human factors and usability engineering to medical devices
  • Usability plan
  • Use specification
  • Usability hazard analysis
  • Use-related hazards
  • User interface specification
  • User interface evaluation plan
  • Preliminary analysis and evaluations
  • Evaluation methods
  • Analytical methods
  • Empirical methods
  • Verification and validation
  • Human factors report
Who will Benefit
  • Development Engineers
  • Production Management
  • QA/QC Personnel
  • Software Developers
  • Usability engineers
  • Risk managers
  • Design Engineering Managers
$375
Recorded Session for one participant
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  • Presentation handouts in downloadable PDF format will be updated on your OCP Account within 24 hours of the purchase of the product
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  • Please share your valuable Feedback at the end of the session
Instructor Profile:
Ed retired from industry after 30 years in management of development of medical device products and development of company Quality Systems. He was involved in the development of products such as IVD devices, kidney dialysis systems and inhalation devices. His QS experience includes, design control, risk analysis, CAPA, software validation, supplier qualification/ control and manufacturing/non-conforming product programs. He now consults in the area of quality systems for medical devices with emphasis on design control, software validation, risk analysis and human factors analysis.

Ed has a B.S. Mechanical Engineering from NYU and a M.B.A from Drexel University. He is certified by Lloyds of London as an ISO 9000 Lead Auditor and is a member of the Thomson Reuters Expert Witness network. He has 5 issued patents.
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