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Best Practices for Medical Device Human Factors Post-Market Surveillance Activities
Best Practices for Medical Device Human Factors Post-Market Surveillance Activities


 
Our Price: $395.00

Product Code: WB-7265
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About the Product
Includes 1 Hour Windows Media Video File and PowerPoint presentations for immediate download.


Regulators and health authorities around the globe are challenging medical device manufacturers to minimize and mitigate adverse events in marketed devices caused by use error through greater post-market surveillance activities. Human factors studies on marketed devices are currently scarce throughout the industry, and human factors teams are seeking opportunities and tested avenues for collecting and analyzing post-market usability data. The following presentation will discuss the challenges and expected outcomes of post-market usability studies, while also highlighting human factors methods for assessing post-market products including contextual inquiries, interviews and observational research.
  • Reviewing applicable regulatory guidance and recommendations
  • Post-market usability study considerations and timetables
  • Making design changes as a result of post-market feedback


Speaker:
Tressa Daniels
Manager of User Experience, Strategic Innovation
Becton Dickinson



Participants that will find this webinar most beneficial will be those involved in medical device companies. Job titles of attendees that will be most applicable for this session will be:
  • Human Factors
  • Usability
  • User Experience/UX
  • Post-market Surveillance

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