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Event :ISO 62366 - How to Conduct a Human Factors

Date :Wednesday April 18th, 2018

Location :Online (Internet, Videoconferencing, ...)

Type :Education - International audience

Accreditation :--


Further information

This webinar will explain the procedure described in ISO62366 and the 
2016 FDA Guidance for a compliant human factors/usability 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:
Engineering Manager
Regulatory Personnel
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 
consulting in the US and internationally in the areas of design control, risk 
analysis and software validation for the past 8 years. Mr. Waldbusser has a 
BS in Mechanical Engineering and an MBA.
Event Fee: One Dial-in One Attendee Price: US$150.00
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Full Details & Registration Link:

Further information

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Compliance4All is a professional trainings provider for the regulated industries. It offers professional trainings for regulatory compliance professionals and offers innovative strategic consulting and advice to a broad range of organizations. These services help them to be compliant with regulatory requirements. . Compliance4All [...]

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ISO 62366 - How to Conduct a Human Factors Medicine - Pharmacy - For the general public
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