2019 Semi-Annual Medical Device Human Factors & Usability Engineering Conference

October 22-23, 2019 | Hilton Alexandria Old Town
December 10-11, 2019 | San Diego, CA

2019 Semi-Annual Medical Device Human Factors & Usability Engineering Conference
October 22-23, 2019 | Hilton Alexandria Old Town
December 10-11, 2019 | San Diego, CA

Download Agenda - Arlington

Download Agenda - San Diego

WE GUARANTEE 100% PRIVACY, YOUR INFORMATION WILL NOT BE SHARED

“I thought the conference was excellent!  Having a conference tailored to one discipline made each panel and contact relevant.”

Director, Compliance & Legal Affairs
Orexigen

“Great insight to hear payer perspective in contracting and account management and the changing healthcare landscape.”

Channel Liaison
Biogen

“It was definitely an excellent well-rounded opportunity to meet new people, get new ideas, and get an in-depth education on what’s to come with the FDA collaborations.”

Quality Engineer
Centurion Medical Products

“It was very well organized event and high quality, the fact to have an IVD track was also interesting. Thanks, I will recommend the Q1 event!”

Regulatory Affairs – EMEA Regional Head
BIOMERIEUX

“The organization and support staff were fantastic! I’m looking forward to next year.”

Global Business Project Lead
Genentech

About the Conference:

Medical device human factors engineering and usability testing executives play an integral role in ensuring medical products can be used safely and intuitively by healthcare professionals, caregivers, and patients, mitigating the risks of user error and meeting increasing FDA regulatory demands surrounding validation of human factors research. Taking a full-lifecycle approach, this meeting not only considers the human factors and user experience research required for product design and development, but also the incorporation of post-market research and feedback on new product iterations as well as changes to products to reduce risks and increase safe usability.

Core Topics to be Addressed:

  • Critical Tasks in Robust Usability Risk Assessment Plans
  • Task Completion Scoring in Device Summative Studies
  • Use Error Requiring Full Design Changes to Devices
  • EU MDR: Human Factors & Usability in Instructions for Use
  • Use of Heuristic Evaluations for Identifying User Risks

Core Topics to be Addressed:

  • Critical Tasks in Robust Usability Risk Assessment Plans
  • Task Completion Scoring in Device Summative Studies
  • Use Error Requiring Full Design Changes to Devices
  • EU MDR: Human Factors & Usability in Instructions for Use
  • Use of Heuristic Evaluations for Identifying User Risks

Download Agenda – Arlington

Download Agenda – San Diego

WE GUARANTEE 100% PRIVACY, YOUR INFORMATION WILL NOT BE SHARED

Audience

75 Attendees

All attendees come directly from medical device companies

Distinguished Presenters

18 Speakers

Networking

Networking time is built into the agenda to allow industry peers to connect and exchange ideas

Open Dialogue and Group Share

Each presentation is followed by 10-15 minutes of open dialogue for questions and exchange of best practices

Share This