ISO 62366 - How to Conduct a Human Factors

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Category Healthcare trainings, medical trainings, food health, healthy courses

Deadline: April 17, 2018 | Date: April 18, 2018

Venue/Country: Online, U.S.A

Updated: 2018-02-20 14:05:16 (GMT+9)

Call For Papers - CFP

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:

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 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

Email: supportcompliance4All.com