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EVENT DATE
Jul 2016
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Human Factors and Usability Studies - By Compliance Global Inc.

Overview

Overview:

Human Factors Usability is the analysis of how people interact with medical devices and medical device risk analysis. The various types and methods of human factors analysis will be explained. This process conforms to the new ISO 62366 standard.

Why Should You Attend:

The FDA will only approve medical devices which are designed so that it is practically impossible for people to accidentally harm themselves even if they use the device improperly. The FDA has replaced the term “user error” with “use error”. This means that use error is considered by the FDA to be a device nonconformity because human factors should be considered in the design process. The burden is on the device designer to create an “idiot proof” product.

Areas Covered in this Webinar:

  • User error versus use error
  • Use related hazards and risk analysis
  • User profiles
  • Use scenarios
  • Step by step human factors program development
  • Validation

Learning Objectives:

Learn how to conduct Human Factors studies and integrate them into your design process

Who Will Benefit:

  • Engineering Personnel
  • QA Personnel
  • Manufacturing Management
  • Management Team

Speaker Profile:

Edwin Waldbusser retired from industry after 30 years in management of development of medical device products and development of company Quality Systems. Products included IVD devices, kidney dialysis systems and inhalation devices.

His QS experience includes design control, risk analysis, CAPA, software validation, supplier qualification/control and manufacturing/non-conforming product programs.

For more detail please click on this below link:

http://bit.ly/1tqTLZt

Email: referrals@complianceglobal.us
Toll Free: +1-844-746-4244
Tel: +1-516-900-5515

Fax: +1-516-900-5510

Notes:
Sponsorship Details:
Compliance Global Inc.

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