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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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The latest industry insights from our global team.
An overview of Emergo by UL’s approach to knowledge tasks to align with FDA expectations.
A look at the European General Product Safety Regulation and its impact on medical device economic operators
A look at our market access and human factors services in the context of comprehensive UL Solutions support for life science and healthcare companies
Medical device usability testing and the emergence of artificial intelligence
Key considerations for conducting self-selection studies for medical devices
A look at the benefits of human factors engineering in consumer product design
Part 2 of our report on key human factors engineering themes at the 2023 HFES conference
Quick Reference Guides (QRG) to help users and patients understand Instructions for Use
Learn more about EU In Vitro Diagnostic Medical Device Regulations.
Learn more about tips and other information to help you feel comfortable when corresponding with the FDA.
Expectations among regulatory bodies are growing just as HFE methods become more and more complex. How will you meet the requirements involved with marketing a medical device?
In this webinar, our Emergo by UL subject matter expert outlines the latest updates on medical device regulatory requirements in South Korea.
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