When: |
13 Apr through 13 Apr 2017 | |
CFP Deadline: |
13 |
|
Where: |
Online Event | United States | |
Website URL: |
http://www.compliance4all.com/control/w_product/~product_id=501208LIVE?channel=mailer&camp=Webinar&AdGroup=brownwalker_Apr_2017_SEO | |
Sponsoring organization: |
Compliance4All | |
Categories: |
Medicine & Health - Medical-Speciality |
Keywords:
Event description:
Overview:
This webinar will explain the procedure described in ISO62366 and the 2016 FDA Guidance for a compliant human factors/ usability validation. HF/U validation is very different from device validation. For example, success criteria is qualitative rather than quantitative as is in device validation.
Why should you Attend:
We will explain how to choose the tests to be conducted and the studies that must be completed prior to the actual validation test. The post test participant inquiry is critical to validation success. we will describe how to do this.
Areas Covered in the Session:
Required number of Participants
Test Procedure
Qualitative Success Criteria
Choice of Tasks to Validate
Post Test Participant Inquiry
Who Will Benefit:
Engineer
Engineering Manager
Regulatory Personnel
QA
Speaker Profile:
Edwin Waldbusser is a consultant retired from industry after 20 years in management of development of medical devices (5 patents). He has been consultin...
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Posting date:
01 March 2017 | 175 views
Placement:
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