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Emergo by UL's new human factors tool - provides training, tools, and resources.
Our software tools offer digital regulatory monitoring for medical device compliance and access to human factors engineering tools.
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TalkingPoints is a round-up of news, insights, and resources about human factors and usability for medical devices, IVDs, combination products, and more.
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Learn about designing effective instructions for medical products, including instructions for use, quick reference guides, package inserts, online help and operator manuals.
Learn about a software user interface (UI) design process that is tailored to the development of medical products of various type.
Learn how to apply human factors engineering to medical products and the HFE process as it is prescribed by regulators and outlined in industry standards.
Learn how to convert the findings from user research into interface requirements.
Learn about HFE reports – what they are, when they are needed, and what they should include.
Gain insight into how people perceive risk, residual risk analysis and its use in medical device development. Sign up for courses on our HFE software platform, OPUS™.
Learn how Root Cause Analysis (RCA) is conducted to discover why problems occurred, and potentially mitigate such occurrences in medical products under development.
Understand usability testing and its key objectives, the differences between various usability tests, and the steps required to conduct usability testing in this course.
Learn how to conduct a known problems analysis (KPA) to gain knowledge that helps eliminate use error vulnerabilities during the development of medical devices.
Gain insight into risk analysis, particularly use-related risk analysis for medical device manufacturers.
Learn how to conduct user research in order to develop safer, easier-to-use medical products in this course.
Understand how HFE's user-centered design process supports the development of safer medical devices.
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