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Writing an Effective Human Factors Engineering Procedure

This webinar discusses the need for medical device companies to create a human factors engineering (HFE) procedure that conforms to current HFE standards as well as the standards and expectations of the FDA and other regulators. Learn how an HFE procedure must be closely tied to a company’s risk management process (e.g., ISO 14971) and ways to turn a general procedure into a detailed and properly scaled one to guide a particular product development effort. This webinar serves the remedial benefit of explaining the purpose of the myriad HFE activities comprising a complete procedure. This webinar will enable audience members to immediately prepare appropriate procedures for their own organization.
$135.00
$225.00
$225.00
Available for Immediate Download

Writing Human Factors Plans and Reports Webinar

This webinar will fill a perceived gap in the guidance available to medical technology developers with sample work products and supplemental job aids that offer document preparation advice and have been peer-reviewed by a panel of HFE experts.
$149.00
$249.00
$249.00
Available for Immediate Download