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Regulatory & Technical Needs of Life Science Usability Pros Met at Human Factors Engineering & Usability Studies Summit

After long delays, 2019 will see the release of new usability standards harmonizing the expectations of FDA and international regulators. What should you expect from these new standards, and how can you begin preparing in advance?

ExL’s 4th Annual Human Factors Engineering & Usability Studies Summit, taking place February 4–5, 2019, in San Francisco, CA, is the only West Coast conference completely devoted to the regulatory and technical needs of life science usability professionals! Our faculty of industry leaders will share all-new analyses not found anywhere else, so save your seat today!

Download The Brochure

Featured Sessions

Post-Brexit Update on International Standards and Harmonization
Ed IsraelskiTechnical Advisor, Human FactorsABBVIE

Pandora’s Box Is a Legacy Product: Working With Add-Ons to Older Devices
Janet LoweSenior Manager, Device Development, Medical AffairsICU MEDICAL

Avoid Regulatory Interventions by Properly Situating Human Factors Testing Within the R&D Life Cycle
John RovnanProduct ManagerZOLL MEDICAL CORPORATION

Why Attend?

  1. Special focus on new domestic and international human factors regulations in a post-Brexit marketplace
  2. Strategies to provide a better sensory experience to users
  3. Improvements for device interoperability
  4. Surefire methods for communicating the ROI of human factors testing to management
  5. Insights on scheduling, sequencing, and budgeting for outsourced human factors tests

To learn more about sponsorship and exhibition opportunities, please contact Christopher Summa at csumma@exlevents.com.

posted in ExL Events News

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