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Within UL Solutions we provide a broad portfolio of offerings to all the medical device industries. This includes certification, Approved/Notified Body and consultancy services. In order to protect and prevent any conflict of interest, perception of conflict of interest and protection of both our brand and our customers brand, we have processes in place to identify and manage any potential conflicts of interest and maintain impartiality. UL Solutions is unable to provide consultancy services to EU MDD, MDR or IVDD Notified Body, UKCA MD Approved Body or MDSAP Customers.
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Human Factors and Usability Software

OPUS™: Digital HFE tools and expertise for medical device design

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For manufacturers of medical devices and technologies, human factors engineering (HFE) and usability are key components when it comes to developing safe and effective products. Many healthcare regulators have established HFE requirements, but building in-house HFE expertise is difficult and time-consuming for many medical device companies.

Our Optimal Product Usability Suite (OPUS™) helps manufacturers leverage cloud-based training, tools, expertise and regulatory guidance in order to meet regulatory HFE expectations as well as incorporate HFE and usability more closely into their product design and development activities.

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