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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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Our global consulting team works from 20+ offices on six continents.
Watch our videos to learn more about the topics that are important to you.
In this video we'll explore the different aspects of a CER including what it is, why it is needed, an overview of the research process, and finally its contents and formatting.
In this video we will learn more about the background of this global quality management system standard, and the steps you can take to obtain ISO 13485 certification in Europe.
Canada is a well-established but lucrative market for medical devices. This 4 minute video explains the medical device registration process in Canada, and the process for gaining approval from Health Canada.
The United States is the number one medical device market in the world. This 4 minute video explains the medical device registration process in the USA, and the process for gaining approval from the FDA.
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