2020 Annual Medical Device Human Factors & Usability Conferences

 October 22-23, 2020 | Arlington, VA

2020 Annual Medical Device Human Factors & Usability Conferences
October 22-23, 2020 | Arlington, VA

Request Invite

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:

Human factors engineering and usability testing for medical device products is an integral component of new product development, and one which must be thoughtfully approached in order to ensure a comprehensive and successful test which provides robust data to support the safe and correct use of technologies, by a wide range of users. From FDA regulatory perspectives on US regulations to notified body perspectives on EU MDR requirements, executives will gain considerable insight and knowledge on best practices in human factor testing to ensure the long-term safety and usability of medical devices.

Core Topics to be Addressed:

  • Tailoring usability tests to include wider ranges of user groups
  • Considerations in testing devices in multiple use scenarios
  • Transforming failed usability tests into device excellence
  • Regulatory requirements with a focus on FDA and EU MDR
  • Innovative case studies featuring the future of usability testing

Program Highlights:

  • High-level case studies from device companies large & small
  • Participation from FDA and Notified Body executives
  • Forward thinking approach for next generation devices & users

Core Topics to be Addressed:

  • Tailoring usability tests to include wider ranges of user groups
  • Considerations in testing devices in multiple use scenarios
  • Transforming failed usability tests into device excellence
  • Regulatory requirements with a focus on FDA and EU MDR
  • Innovative case studies featuring the future of usability testing

Request Invite

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

Audience

75 Attendees

All attendees come directly from medical device companies

Distinguished Presenters

Speaker recruitment in progress

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

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